Canonical Allele Identifier: CA340133862

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 1758065
• ClinVar RCV Id: RCV003614132 ; RCV002382640
• dbSNP Id: rs1644931388
• gnomAD v3: 1-45331827-G-C
• gnomAD v4: 1-45331827-G-C
• MyVariant Identifiers: chr1:g.45797499G>C (hg19) ; chr1:g.45331827G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331827G>C , CM000663.2:g.45331827G>C	GRCh38
NC_000001.10:g.45797499G>C , CM000663.1:g.45797499G>C	GRCh37
NC_000001.9:g.45570086G>C	NCBI36
NG_008189.1:g.13644C>G , LRG_220:g.13644C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.552C>G	ENSP00000410263.2:p.His184Gln
ENST00000435155.2:c.969C>G	ENSP00000403655.2:p.His323Gln
ENST00000467459.6:c.959C>G	ENSP00000435889.2:p.Thr320Ser
ENST00000483127.2:c.954C>G	ENSP00000436469.2:p.His318Gln
ENST00000485271.6:c.936C>G	ENSP00000431264.2:p.His312Gln
ENST00000529892.6:c.955+196C>G	ENSP00000432528.2:n.955+196C>G
ENST00000533178.6:c.*265C>G	ENSP00000436430.2:n.*265C>G
ENST00000672314.2:c.936C>G	ENSP00000500828.2:p.His312Gln
ENST00000710952.2:c.1020C>G MANE Plus Clinical	ENSP00000518552.2:p.His340Gln
ENST00000672818.3:c.1011C>G	ENSP00000500891.1:p.His337Gln
ENST00000456914.7:c.936C>G MANE Select	ENSP00000407590.2:p.His312Gln
ENST00000671898.1:c.1524C>G	ENSP00000499896.1:p.His508Gln
ENST00000672011.1:c.*265C>G	ENSP00000500418.1:n.*265C>G
ENST00000672314.1:c.936C>G	ENSP00000500828.1:p.His312Gln
ENST00000672593.1:c.*1162C>G	ENSP00000500455.1:n.*1162C>G
ENST00000672764.1:c.*265C>G	ENSP00000500886.1:n.*265C>G
ENST00000672818.2:c.1011C>G	ENSP00000500891.1:p.His337Gln
ENST00000673134.1:c.*633C>G	ENSP00000500526.1:n.*633C>G
ENST00000354383.10:c.939C>G	ENSP00000346354.6:p.His313Gln
ENST00000355498.6:c.936C>G	ENSP00000347685.2:p.His312Gln
ENST00000372098.7:c.1011C>G	ENSP00000361170.3:p.His337Gln
ENST00000372104.5:c.936C>G	ENSP00000361176.1:p.His312Gln
ENST00000372110.7:c.981C>G	ENSP00000361182.3:p.His327Gln
ENST00000372115.7:c.978C>G	ENSP00000361187.3:p.His326Gln
ENST00000412971.5:c.552C>G	ENSP00000410263.1:p.His184Gln
ENST00000448481.5:c.969C>G	ENSP00000409718.1:p.His323Gln
ENST00000450313.5:c.1020C>G	ENSP00000408176.1:p.His340Gln
ENST00000456914.6:c.936C>G	ENSP00000407590.2:p.His312Gln
ENST00000462388.5:n.800C>G
ENST00000466231.1:n.301C>G
ENST00000467459.5:c.353C>G	ENSP00000435889.1:p.Thr118Ser
ENST00000475516.5:c.*749C>G	ENSP00000433843.1:n.*749C>G
ENST00000481571.5:c.*749C>G	ENSP00000436597.1:n.*749C>G
ENST00000482094.5:n.257C>G
ENST00000488731.6:c.188-271C>G	ENSP00000432330.1:n.188-271C>G
ENST00000528013.6:c.978C>G	ENSP00000433130.2:p.His326Gln
ENST00000529892.5:c.177+196C>G
ENST00000529984.5:c.188-271C>G	ENSP00000437093.1:n.188-271C>G
ENST00000531105.5:c.116-2390C>G	ENSP00000431292.1:n.116-2390C>G
ENST00000533178.5:c.565C>G	ENSP00000436430.1:n.565C>G
NM_001048171.1:c.978C>G	NP_001041636.1:p.His326Gln
NM_001048172.1:c.939C>G	NP_001041637.1:p.His313Gln
NM_001048173.1:c.936C>G	NP_001041638.1:p.His312Gln
NM_001048174.1:c.936C>G	NP_001041639.1:p.His312Gln
NM_001128425.1:c.1020C>G , LRG_220t1:c.1020C>G	NP_001121897.1:p.His340Gln
NM_001293190.1:c.981C>G	NP_001280119.1:p.His327Gln
NM_001293191.1:c.969C>G	NP_001280120.1:p.His323Gln
NM_001293192.1:c.660C>G	NP_001280121.1:p.His220Gln
NM_001293195.1:c.936C>G	NP_001280124.1:p.His312Gln
NM_001293196.1:c.660C>G	NP_001280125.1:p.His220Gln
NM_012222.2:c.1011C>G	NP_036354.1:p.His337Gln
XM_011541497.1:c.996C>G	XP_011539799.1:p.His332Gln
XM_011541498.1:c.978C>G	XP_011539800.1:p.His326Gln
XM_011541499.1:c.978C>G	XP_011539801.1:p.His326Gln
XM_011541500.1:c.978C>G	XP_011539802.1:p.His326Gln
XM_011541501.1:c.978C>G	XP_011539803.1:p.His326Gln
XM_011541502.1:c.978C>G	XP_011539804.1:p.His326Gln
XM_011541503.1:c.978C>G	XP_011539805.1:p.His326Gln
XM_011541504.1:c.969C>G	XP_011539806.1:p.His323Gln
XM_011541505.1:c.558C>G	XP_011539807.1:p.His186Gln
XM_011541506.1:c.558C>G	XP_011539808.1:p.His186Gln
XM_011541507.1:c.549C>G	XP_011539809.1:p.His183Gln
XM_011541508.1:c.564C>G	XP_011539810.1:p.His188Gln
XR_946658.1:n.1067C>G
NM_001350650.1:c.591C>G	NP_001337579.1:p.His197Gln
NM_001350651.1:c.591C>G	NP_001337580.1:p.His197Gln
NR_146882.1:n.1194C>G
NR_146883.1:n.1008C>G
XM_011541497.3:c.996C>G	XP_011539799.1:p.His332Gln
XM_011541500.3:c.978C>G	XP_011539802.1:p.His326Gln
XM_011541501.2:c.978C>G	XP_011539803.1:p.His326Gln
XM_011541502.2:c.978C>G	XP_011539804.1:p.His326Gln
XM_011541503.2:c.978C>G	XP_011539805.1:p.His326Gln
XM_011541504.2:c.969C>G	XP_011539806.1:p.His323Gln
XM_011541505.2:c.558C>G	XP_011539807.1:p.His186Gln
XM_011541506.2:c.558C>G	XP_011539808.1:p.His186Gln
XM_017001331.1:c.978C>G	XP_016856820.1:p.His326Gln
XM_017001332.1:c.978C>G	XP_016856821.1:p.His326Gln
XM_017001333.1:c.978C>G	XP_016856822.1:p.His326Gln
XM_017001334.1:c.939C>G	XP_016856823.1:p.His313Gln
XM_017001335.1:c.660C>G	XP_016856824.1:p.His220Gln
XM_017001336.1:c.591C>G	XP_016856825.1:p.His197Gln
XM_017001337.1:c.591C>G	XP_016856826.1:p.His197Gln
XM_024447244.1:c.591C>G	XP_024303012.1:p.His197Gln
XM_024447245.1:c.591C>G	XP_024303013.1:p.His197Gln
XM_024447248.1:c.549C>G	XP_024303016.1:p.His183Gln
XM_024447249.1:c.420C>G	XP_024303017.1:p.His140Gln
XM_024447250.1:c.420C>G	XP_024303018.1:p.His140Gln
XM_024447251.1:c.420C>G	XP_024303019.1:p.His140Gln
XR_001737190.1:n.981C>G
XR_001737192.1:n.793C>G
XR_002956643.1:n.973C>G
XR_002956644.1:n.1508C>G
XR_946658.2:n.1081C>G
NM_001048171.2:c.936C>G	NP_001041636.2:p.His312Gln
NM_001128425.2:c.1020C>G MANE Plus Clinical	NP_001121897.1:p.His340Gln
NM_001048172.2:c.939C>G	NP_001041637.1:p.His313Gln
NM_001048173.2:c.936C>G	NP_001041638.1:p.His312Gln
NM_001048174.2:c.936C>G MANE Select	NP_001041639.1:p.His312Gln
NM_001293190.2:c.981C>G	NP_001280119.1:p.His327Gln
NM_001293191.2:c.969C>G	NP_001280120.1:p.His323Gln
NM_001293192.2:c.660C>G	NP_001280121.1:p.His220Gln
NM_001293195.2:c.936C>G	NP_001280124.1:p.His312Gln
NM_001293196.2:c.660C>G	NP_001280125.1:p.His220Gln
NM_001350650.2:c.591C>G	NP_001337579.1:p.His197Gln
NM_001350651.2:c.591C>G	NP_001337580.1:p.His197Gln
NM_012222.3:c.1011C>G	NP_036354.1:p.His337Gln
NR_146882.2:n.1164C>G
NR_146883.2:n.1013C>G