Canonical Allele Identifier: CA058637

Gene: MUTYH

Linked Data

• dbSNP Id: rs775300564
• ExAC: 1:45798220 A / C
• gnomAD v2: 1-45798220-A-C
• MyVariant Identifiers: chr1:g.45798220A>C (hg19) ; chr1:g.45332548A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332548A>C , CM000663.2:g.45332548A>C	GRCh38
NC_000001.10:g.45798220A>C , CM000663.1:g.45798220A>C	GRCh37
NC_000001.9:g.45570807A>C	NCBI36
NG_008189.1:g.12923T>G , LRG_220:g.12923T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.222+26T>G	ENSP00000410263.2:n.222+26T>G
ENST00000435155.2:c.639+26T>G	ENSP00000403655.2:n.639+26T>G
ENST00000467459.6:c.606+26T>G	ENSP00000435889.2:n.606+26T>G
ENST00000483127.2:c.624+26T>G	ENSP00000436469.2:n.624+26T>G
ENST00000485271.6:c.606+26T>G	ENSP00000431264.2:n.606+26T>G
ENST00000529892.6:c.648+26T>G	ENSP00000432528.2:n.648+26T>G
ENST00000533178.6:c.229+26T>G	ENSP00000436430.2:n.229+26T>G
ENST00000672314.2:c.606+26T>G	ENSP00000500828.2:n.606+26T>G
ENST00000674679.2:c.*518+26T>G	ENSP00000501623.2:n.*518+26T>G
ENST00000710952.2:c.690+26T>G MANE Plus Clinical	ENSP00000518552.2:n.690+26T>G
ENST00000672818.3:c.681+26T>G	ENSP00000500891.1:n.681+26T>G
ENST00000450313.6:c.616+26T>G	ENSP00000408176.2:n.616+26T>G
ENST00000456914.7:c.606+26T>G MANE Select	ENSP00000407590.2:n.606+26T>G
ENST00000461495.6:c.*345+26T>G	ENSP00000437166.1:n.*345+26T>G
ENST00000671898.1:c.1194+26T>G	ENSP00000499896.1:n.1194+26T>G
ENST00000672011.1:c.574+26T>G	ENSP00000500418.1:n.574+26T>G
ENST00000672314.1:c.606+26T>G	ENSP00000500828.1:n.606+26T>G
ENST00000672593.1:c.*520T>G	ENSP00000500455.1:n.*520T>G
ENST00000672764.1:c.565+26T>G	ENSP00000500886.1:n.565+26T>G
ENST00000672818.2:c.681+26T>G	ENSP00000500891.1:n.681+26T>G
ENST00000673134.1:c.*303+26T>G	ENSP00000500526.1:n.*303+26T>G
ENST00000674679.1:c.634+26T>G	ENSP00000501623.1:n.634+26T>G
ENST00000354383.10:c.609+26T>G	ENSP00000346354.6:n.609+26T>G
ENST00000355498.6:c.606+26T>G	ENSP00000347685.2:n.606+26T>G
ENST00000372098.7:c.681+26T>G	ENSP00000361170.3:n.681+26T>G
ENST00000372104.5:c.606+26T>G	ENSP00000361176.1:n.606+26T>G
ENST00000372110.7:c.651+26T>G	ENSP00000361182.3:n.651+26T>G
ENST00000372115.7:c.648+26T>G	ENSP00000361187.3:n.648+26T>G
ENST00000412971.5:c.222+26T>G	ENSP00000410263.1:n.222+26T>G
ENST00000435155.1:c.639+26T>G	ENSP00000403655.1:n.639+26T>G
ENST00000448481.5:c.639+26T>G	ENSP00000409718.1:n.639+26T>G
ENST00000450313.5:c.690+26T>G	ENSP00000408176.1:n.690+26T>G
ENST00000456914.6:c.606+26T>G	ENSP00000407590.2:n.606+26T>G
ENST00000461495.5:c.*345+26T>G	ENSP00000437166.1:n.*345+26T>G
ENST00000462388.5:n.297+26T>G
ENST00000467940.5:c.*529+26T>G	ENSP00000436478.1:n.*529+26T>G
ENST00000470256.5:c.493+26T>G	ENSP00000434985.1:n.493+26T>G
ENST00000475516.5:c.*419+26T>G	ENSP00000433843.1:n.*419+26T>G
ENST00000478796.5:n.593+26T>G
ENST00000481571.5:c.*419+26T>G	ENSP00000436597.1:n.*419+26T>G
ENST00000488731.6:c.187+215T>G	ENSP00000432330.1:n.187+215T>G
ENST00000525160.5:c.*257+26T>G	ENSP00000431568.1:n.*257+26T>G
ENST00000528013.6:c.648+26T>G	ENSP00000433130.2:n.648+26T>G
ENST00000529984.5:c.187+215T>G	ENSP00000437093.1:n.187+215T>G
ENST00000531105.5:c.115+1843T>G	ENSP00000431292.1:n.115+1843T>G
ENST00000533178.5:c.235+26T>G	ENSP00000436430.1:n.235+26T>G
NM_001048171.1:c.648+26T>G	NP_001041636.1:n.648+26T>G
NM_001048172.1:c.609+26T>G	NP_001041637.1:n.609+26T>G
NM_001048173.1:c.606+26T>G	NP_001041638.1:n.606+26T>G
NM_001048174.1:c.606+26T>G	NP_001041639.1:n.606+26T>G
NM_001128425.1:c.690+26T>G , LRG_220t1:c.690+26T>G	NP_001121897.1:n.690+26T>G
NM_001293190.1:c.651+26T>G	NP_001280119.1:n.651+26T>G
NM_001293191.1:c.639+26T>G	NP_001280120.1:n.639+26T>G
NM_001293192.1:c.330+26T>G	NP_001280121.1:n.330+26T>G
NM_001293195.1:c.606+26T>G	NP_001280124.1:n.606+26T>G
NM_001293196.1:c.330+26T>G	NP_001280125.1:n.330+26T>G
NM_012222.2:c.681+26T>G	NP_036354.1:n.681+26T>G
XM_011541497.1:c.666+26T>G	XP_011539799.1:n.666+26T>G
XM_011541498.1:c.648+26T>G	XP_011539800.1:n.648+26T>G
XM_011541499.1:c.648+26T>G	XP_011539801.1:n.648+26T>G
XM_011541500.1:c.648+26T>G	XP_011539802.1:n.648+26T>G
XM_011541501.1:c.648+26T>G	XP_011539803.1:n.648+26T>G
XM_011541502.1:c.648+26T>G	XP_011539804.1:n.648+26T>G
XM_011541503.1:c.648+26T>G	XP_011539805.1:n.648+26T>G
XM_011541504.1:c.639+26T>G	XP_011539806.1:n.639+26T>G
XM_011541505.1:c.228+26T>G	XP_011539807.1:n.228+26T>G
XM_011541506.1:c.228+26T>G	XP_011539808.1:n.228+26T>G
XM_011541507.1:c.219+26T>G	XP_011539809.1:n.219+26T>G
XM_011541508.1:c.234+26T>G	XP_011539810.1:n.234+26T>G
XR_946658.1:n.737+26T>G
NM_001350650.1:c.261+26T>G	NP_001337579.1:n.261+26T>G
NM_001350651.1:c.261+26T>G	NP_001337580.1:n.261+26T>G
NR_146882.1:n.864+26T>G
NR_146883.1:n.678+26T>G
XM_011541497.3:c.666+26T>G	XP_011539799.1:n.666+26T>G
XM_011541500.3:c.648+26T>G	XP_011539802.1:n.648+26T>G
XM_011541501.2:c.648+26T>G	XP_011539803.1:n.648+26T>G
XM_011541502.2:c.648+26T>G	XP_011539804.1:n.648+26T>G
XM_011541503.2:c.648+26T>G	XP_011539805.1:n.648+26T>G
XM_011541504.2:c.639+26T>G	XP_011539806.1:n.639+26T>G
XM_011541505.2:c.228+26T>G	XP_011539807.1:n.228+26T>G
XM_011541506.2:c.228+26T>G	XP_011539808.1:n.228+26T>G
XM_017001331.1:c.648+26T>G	XP_016856820.1:n.648+26T>G
XM_017001332.1:c.648+26T>G	XP_016856821.1:n.648+26T>G
XM_017001333.1:c.648+26T>G	XP_016856822.1:n.648+26T>G
XM_017001334.1:c.609+26T>G	XP_016856823.1:n.609+26T>G
XM_017001335.1:c.330+26T>G	XP_016856824.1:n.330+26T>G
XM_017001336.1:c.261+26T>G	XP_016856825.1:n.261+26T>G
XM_017001337.1:c.261+26T>G	XP_016856826.1:n.261+26T>G
XM_024447244.1:c.261+26T>G	XP_024303012.1:n.261+26T>G
XM_024447245.1:c.261+26T>G	XP_024303013.1:n.261+26T>G
XM_024447248.1:c.219+26T>G	XP_024303016.1:n.219+26T>G
XM_024447249.1:c.90+26T>G	XP_024303017.1:n.90+26T>G
XM_024447250.1:c.90+26T>G	XP_024303018.1:n.90+26T>G
XM_024447251.1:c.90+26T>G	XP_024303019.1:n.90+26T>G
XR_001737190.1:n.651+26T>G
XR_001737192.1:n.463+26T>G
XR_002956643.1:n.643+26T>G
XR_002956644.1:n.1178+26T>G
XR_946658.2:n.751+26T>G
NM_001048171.2:c.606+26T>G	NP_001041636.2:n.606+26T>G
NM_001128425.2:c.690+26T>G MANE Plus Clinical	NP_001121897.1:n.690+26T>G
NM_001048172.2:c.609+26T>G	NP_001041637.1:n.609+26T>G
NM_001048173.2:c.606+26T>G	NP_001041638.1:n.606+26T>G
NM_001048174.2:c.606+26T>G MANE Select	NP_001041639.1:n.606+26T>G
NM_001293190.2:c.651+26T>G	NP_001280119.1:n.651+26T>G
NM_001293191.2:c.639+26T>G	NP_001280120.1:n.639+26T>G
NM_001293192.2:c.330+26T>G	NP_001280121.1:n.330+26T>G
NM_001293195.2:c.606+26T>G	NP_001280124.1:n.606+26T>G
NM_001293196.2:c.330+26T>G	NP_001280125.1:n.330+26T>G
NM_001350650.2:c.261+26T>G	NP_001337579.1:n.261+26T>G
NM_001350651.2:c.261+26T>G	NP_001337580.1:n.261+26T>G
NM_012222.3:c.681+26T>G	NP_036354.1:n.681+26T>G
NR_146882.2:n.834+26T>G
NR_146883.2:n.683+26T>G