Canonical Allele Identifier: CA340134688

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 492061
• ClinVar RCV Id: RCV000581418
• dbSNP Id: rs1331273811
• MyVariant Identifiers: chr1:g.45797962A>C (hg19) ; chr1:g.45332290A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332290A>C , CM000663.2:g.45332290A>C	GRCh38
NC_000001.10:g.45797962A>C , CM000663.1:g.45797962A>C	GRCh37
NC_000001.9:g.45570549A>C	NCBI36
NG_008189.1:g.13181T>G , LRG_220:g.13181T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.341T>G	ENSP00000410263.2:p.Val114Gly
ENST00000435155.2:c.758T>G	ENSP00000403655.2:p.Val253Gly
ENST00000467459.6:c.725T>G	ENSP00000435889.2:p.Val242Gly
ENST00000483127.2:c.743T>G	ENSP00000436469.2:p.Val248Gly
ENST00000485271.6:c.725T>G	ENSP00000431264.2:p.Val242Gly
ENST00000529892.6:c.767T>G	ENSP00000432528.2:p.Val256Gly
ENST00000533178.6:c.*54T>G	ENSP00000436430.2:n.*54T>G
ENST00000672314.2:c.725T>G	ENSP00000500828.2:p.Val242Gly
ENST00000674679.2:c.*637T>G	ENSP00000501623.2:n.*637T>G
ENST00000710952.2:c.809T>G MANE Plus Clinical	ENSP00000518552.2:p.Val270Gly
ENST00000672818.3:c.800T>G	ENSP00000500891.1:p.Val267Gly
ENST00000450313.6:c.*54T>G	ENSP00000408176.2:n.*54T>G
ENST00000456914.7:c.725T>G MANE Select	ENSP00000407590.2:p.Val242Gly
ENST00000461495.6:c.*464T>G	ENSP00000437166.1:n.*464T>G
ENST00000671898.1:c.1313T>G	ENSP00000499896.1:p.Val438Gly
ENST00000672011.1:c.*54T>G	ENSP00000500418.1:n.*54T>G
ENST00000672314.1:c.725T>G	ENSP00000500828.1:p.Val242Gly
ENST00000672593.1:c.*778T>G	ENSP00000500455.1:n.*778T>G
ENST00000672764.1:c.*54T>G	ENSP00000500886.1:n.*54T>G
ENST00000672818.2:c.800T>G	ENSP00000500891.1:p.Val267Gly
ENST00000673134.1:c.*422T>G	ENSP00000500526.1:n.*422T>G
ENST00000674679.1:c.753T>G	ENSP00000501623.1:n.753T>G
ENST00000354383.10:c.728T>G	ENSP00000346354.6:p.Val243Gly
ENST00000355498.6:c.725T>G	ENSP00000347685.2:p.Val242Gly
ENST00000372098.7:c.800T>G	ENSP00000361170.3:p.Val267Gly
ENST00000372104.5:c.725T>G	ENSP00000361176.1:p.Val242Gly
ENST00000372110.7:c.770T>G	ENSP00000361182.3:p.Val257Gly
ENST00000372115.7:c.767T>G	ENSP00000361187.3:p.Val256Gly
ENST00000412971.5:c.341T>G	ENSP00000410263.1:p.Val114Gly
ENST00000435155.1:c.758T>G	ENSP00000403655.1:p.Val253Gly
ENST00000448481.5:c.758T>G	ENSP00000409718.1:p.Val253Gly
ENST00000450313.5:c.809T>G	ENSP00000408176.1:p.Val270Gly
ENST00000456914.6:c.725T>G	ENSP00000407590.2:p.Val242Gly
ENST00000461495.5:c.*464T>G	ENSP00000437166.1:n.*464T>G
ENST00000462388.5:n.416T>G
ENST00000466231.1:n.90T>G
ENST00000467459.5:c.119T>G	ENSP00000435889.1:p.Val40Gly
ENST00000467940.5:c.*648T>G	ENSP00000436478.1:n.*648T>G
ENST00000470256.5:c.*54T>G	ENSP00000434985.1:n.*54T>G
ENST00000475516.5:c.*538T>G	ENSP00000433843.1:n.*538T>G
ENST00000478796.5:n.712T>G
ENST00000481571.5:c.*538T>G	ENSP00000436597.1:n.*538T>G
ENST00000488731.6:c.187+473T>G	ENSP00000432330.1:n.187+473T>G
ENST00000528013.6:c.767T>G	ENSP00000433130.2:p.Val256Gly
ENST00000529984.5:c.187+473T>G	ENSP00000437093.1:n.187+473T>G
ENST00000531105.5:c.115+2101T>G	ENSP00000431292.1:n.115+2101T>G
ENST00000533178.5:c.354T>G	ENSP00000436430.1:n.354T>G
NM_001048171.1:c.767T>G	NP_001041636.1:p.Val256Gly
NM_001048172.1:c.728T>G	NP_001041637.1:p.Val243Gly
NM_001048173.1:c.725T>G	NP_001041638.1:p.Val242Gly
NM_001048174.1:c.725T>G	NP_001041639.1:p.Val242Gly
NM_001128425.1:c.809T>G , LRG_220t1:c.809T>G	NP_001121897.1:p.Val270Gly
NM_001293190.1:c.770T>G	NP_001280119.1:p.Val257Gly
NM_001293191.1:c.758T>G	NP_001280120.1:p.Val253Gly
NM_001293192.1:c.449T>G	NP_001280121.1:p.Val150Gly
NM_001293195.1:c.725T>G	NP_001280124.1:p.Val242Gly
NM_001293196.1:c.449T>G	NP_001280125.1:p.Val150Gly
NM_012222.2:c.800T>G	NP_036354.1:p.Val267Gly
XM_011541497.1:c.785T>G	XP_011539799.1:p.Val262Gly
XM_011541498.1:c.767T>G	XP_011539800.1:p.Val256Gly
XM_011541499.1:c.767T>G	XP_011539801.1:p.Val256Gly
XM_011541500.1:c.767T>G	XP_011539802.1:p.Val256Gly
XM_011541501.1:c.767T>G	XP_011539803.1:p.Val256Gly
XM_011541502.1:c.767T>G	XP_011539804.1:p.Val256Gly
XM_011541503.1:c.767T>G	XP_011539805.1:p.Val256Gly
XM_011541504.1:c.758T>G	XP_011539806.1:p.Val253Gly
XM_011541505.1:c.347T>G	XP_011539807.1:p.Val116Gly
XM_011541506.1:c.347T>G	XP_011539808.1:p.Val116Gly
XM_011541507.1:c.338T>G	XP_011539809.1:p.Val113Gly
XM_011541508.1:c.353T>G	XP_011539810.1:p.Val118Gly
XR_946658.1:n.856T>G
NM_001350650.1:c.380T>G	NP_001337579.1:p.Val127Gly
NM_001350651.1:c.380T>G	NP_001337580.1:p.Val127Gly
NR_146882.1:n.983T>G
NR_146883.1:n.797T>G
XM_011541497.3:c.785T>G	XP_011539799.1:p.Val262Gly
XM_011541500.3:c.767T>G	XP_011539802.1:p.Val256Gly
XM_011541501.2:c.767T>G	XP_011539803.1:p.Val256Gly
XM_011541502.2:c.767T>G	XP_011539804.1:p.Val256Gly
XM_011541503.2:c.767T>G	XP_011539805.1:p.Val256Gly
XM_011541504.2:c.758T>G	XP_011539806.1:p.Val253Gly
XM_011541505.2:c.347T>G	XP_011539807.1:p.Val116Gly
XM_011541506.2:c.347T>G	XP_011539808.1:p.Val116Gly
XM_017001331.1:c.767T>G	XP_016856820.1:p.Val256Gly
XM_017001332.1:c.767T>G	XP_016856821.1:p.Val256Gly
XM_017001333.1:c.767T>G	XP_016856822.1:p.Val256Gly
XM_017001334.1:c.728T>G	XP_016856823.1:p.Val243Gly
XM_017001335.1:c.449T>G	XP_016856824.1:p.Val150Gly
XM_017001336.1:c.380T>G	XP_016856825.1:p.Val127Gly
XM_017001337.1:c.380T>G	XP_016856826.1:p.Val127Gly
XM_024447244.1:c.380T>G	XP_024303012.1:p.Val127Gly
XM_024447245.1:c.380T>G	XP_024303013.1:p.Val127Gly
XM_024447248.1:c.338T>G	XP_024303016.1:p.Val113Gly
XM_024447249.1:c.209T>G	XP_024303017.1:p.Val70Gly
XM_024447250.1:c.209T>G	XP_024303018.1:p.Val70Gly
XM_024447251.1:c.209T>G	XP_024303019.1:p.Val70Gly
XR_001737190.1:n.770T>G
XR_001737192.1:n.582T>G
XR_002956643.1:n.762T>G
XR_002956644.1:n.1297T>G
XR_946658.2:n.870T>G
NM_001048171.2:c.725T>G	NP_001041636.2:p.Val242Gly
NM_001128425.2:c.809T>G MANE Plus Clinical	NP_001121897.1:p.Val270Gly
NM_001048172.2:c.728T>G	NP_001041637.1:p.Val243Gly
NM_001048173.2:c.725T>G	NP_001041638.1:p.Val242Gly
NM_001048174.2:c.725T>G MANE Select	NP_001041639.1:p.Val242Gly
NM_001293190.2:c.770T>G	NP_001280119.1:p.Val257Gly
NM_001293191.2:c.758T>G	NP_001280120.1:p.Val253Gly
NM_001293192.2:c.449T>G	NP_001280121.1:p.Val150Gly
NM_001293195.2:c.725T>G	NP_001280124.1:p.Val242Gly
NM_001293196.2:c.449T>G	NP_001280125.1:p.Val150Gly
NM_001350650.2:c.380T>G	NP_001337579.1:p.Val127Gly
NM_001350651.2:c.380T>G	NP_001337580.1:p.Val127Gly
NM_012222.3:c.800T>G	NP_036354.1:p.Val267Gly
NR_146882.2:n.953T>G
NR_146883.2:n.802T>G