Canonical Allele Identifier: CA340135377

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 1368442
• ClinVar RCV Id: RCV001874411 ; RCV002359317
• dbSNP Id: rs2149151527
• gnomAD v4: 1-45332639-G-A
• MyVariant Identifiers: chr1:g.45798311G>A (hg19) ; chr1:g.45332639G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332639G>A , CM000663.2:g.45332639G>A	GRCh38
NC_000001.10:g.45798311G>A , CM000663.1:g.45798311G>A	GRCh37
NC_000001.9:g.45570898G>A	NCBI36
NG_008189.1:g.12832C>T , LRG_220:g.12832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.157C>T	ENSP00000410263.2:p.Gln53Ter
ENST00000435155.2:c.574C>T	ENSP00000403655.2:p.Gln192Ter
ENST00000467459.6:c.541C>T	ENSP00000435889.2:p.Gln181Ter
ENST00000483127.2:c.559C>T	ENSP00000436469.2:p.Gln187Ter
ENST00000485271.6:c.541C>T	ENSP00000431264.2:p.Gln181Ter
ENST00000529892.6:c.583C>T	ENSP00000432528.2:p.Gln195Ter
ENST00000533178.6:c.164C>T	ENSP00000436430.2:p.Ala55Val
ENST00000672314.2:c.541C>T	ENSP00000500828.2:p.Gln181Ter
ENST00000674679.2:c.*453C>T	ENSP00000501623.2:n.*453C>T
ENST00000710952.2:c.625C>T MANE Plus Clinical	ENSP00000518552.2:p.Gln209Ter
ENST00000672818.3:c.616C>T	ENSP00000500891.1:p.Gln206Ter
ENST00000450313.6:c.551C>T	ENSP00000408176.2:p.Ala184Val
ENST00000456914.7:c.541C>T MANE Select	ENSP00000407590.2:p.Gln181Ter
ENST00000461495.6:c.*280C>T	ENSP00000437166.1:n.*280C>T
ENST00000671856.1:n.487C>T
ENST00000671898.1:c.1129C>T	ENSP00000499896.1:p.Gln377Ter
ENST00000672011.1:c.509C>T	ENSP00000500418.1:p.Ala170Val
ENST00000672314.1:c.541C>T	ENSP00000500828.1:p.Gln181Ter
ENST00000672593.1:c.*429C>T	ENSP00000500455.1:n.*429C>T
ENST00000672764.1:c.500C>T	ENSP00000500886.1:p.Ala167Val
ENST00000672818.2:c.616C>T	ENSP00000500891.1:p.Gln206Ter
ENST00000673134.1:c.*238C>T	ENSP00000500526.1:n.*238C>T
ENST00000674679.1:c.569C>T	ENSP00000501623.1:n.569C>T
ENST00000354383.10:c.544C>T	ENSP00000346354.6:p.Gln182Ter
ENST00000355498.6:c.541C>T	ENSP00000347685.2:p.Gln181Ter
ENST00000372098.7:c.616C>T	ENSP00000361170.3:p.Gln206Ter
ENST00000372104.5:c.541C>T	ENSP00000361176.1:p.Gln181Ter
ENST00000372110.7:c.586C>T	ENSP00000361182.3:p.Gln196Ter
ENST00000372115.7:c.583C>T	ENSP00000361187.3:p.Gln195Ter
ENST00000412971.5:c.157C>T	ENSP00000410263.1:p.Gln53Ter
ENST00000435155.1:c.574C>T	ENSP00000403655.1:p.Gln192Ter
ENST00000448481.5:c.574C>T	ENSP00000409718.1:p.Gln192Ter
ENST00000450313.5:c.625C>T	ENSP00000408176.1:p.Gln209Ter
ENST00000456914.6:c.541C>T	ENSP00000407590.2:p.Gln181Ter
ENST00000461495.5:c.*280C>T	ENSP00000437166.1:n.*280C>T
ENST00000462388.5:n.232C>T
ENST00000467940.5:c.*464C>T	ENSP00000436478.1:n.*464C>T
ENST00000470256.5:c.428C>T	ENSP00000434985.1:p.Ala143Val
ENST00000475516.5:c.*354C>T	ENSP00000433843.1:n.*354C>T
ENST00000478796.5:n.528C>T
ENST00000479746.6:n.899C>T
ENST00000481571.5:c.*354C>T	ENSP00000436597.1:n.*354C>T
ENST00000483642.5:n.1056C>T
ENST00000488731.6:c.187+124C>T	ENSP00000432330.1:n.187+124C>T
ENST00000492494.5:n.938C>T
ENST00000525160.5:c.*192C>T	ENSP00000431568.1:n.*192C>T
ENST00000528013.6:c.583C>T	ENSP00000433130.2:p.Gln195Ter
ENST00000529984.5:c.187+124C>T	ENSP00000437093.1:n.187+124C>T
ENST00000531105.5:c.115+1752C>T	ENSP00000431292.1:n.115+1752C>T
ENST00000533178.5:c.170C>T	ENSP00000436430.1:p.Ala57Val
NM_001048171.1:c.583C>T	NP_001041636.1:p.Gln195Ter
NM_001048172.1:c.544C>T	NP_001041637.1:p.Gln182Ter
NM_001048173.1:c.541C>T	NP_001041638.1:p.Gln181Ter
NM_001048174.1:c.541C>T	NP_001041639.1:p.Gln181Ter
NM_001128425.1:c.625C>T , LRG_220t1:c.625C>T	NP_001121897.1:p.Gln209Ter
NM_001293190.1:c.586C>T	NP_001280119.1:p.Gln196Ter
NM_001293191.1:c.574C>T	NP_001280120.1:p.Gln192Ter
NM_001293192.1:c.265C>T	NP_001280121.1:p.Gln89Ter
NM_001293195.1:c.541C>T	NP_001280124.1:p.Gln181Ter
NM_001293196.1:c.265C>T	NP_001280125.1:p.Gln89Ter
NM_012222.2:c.616C>T	NP_036354.1:p.Gln206Ter
XM_011541497.1:c.601C>T	XP_011539799.1:p.Gln201Ter
XM_011541498.1:c.583C>T	XP_011539800.1:p.Gln195Ter
XM_011541499.1:c.583C>T	XP_011539801.1:p.Gln195Ter
XM_011541500.1:c.583C>T	XP_011539802.1:p.Gln195Ter
XM_011541501.1:c.583C>T	XP_011539803.1:p.Gln195Ter
XM_011541502.1:c.583C>T	XP_011539804.1:p.Gln195Ter
XM_011541503.1:c.583C>T	XP_011539805.1:p.Gln195Ter
XM_011541504.1:c.574C>T	XP_011539806.1:p.Gln192Ter
XM_011541505.1:c.163C>T	XP_011539807.1:p.Gln55Ter
XM_011541506.1:c.163C>T	XP_011539808.1:p.Gln55Ter
XM_011541507.1:c.154C>T	XP_011539809.1:p.Gln52Ter
XM_011541508.1:c.169C>T	XP_011539810.1:p.Gln57Ter
XR_946658.1:n.672C>T
NM_001350650.1:c.196C>T	NP_001337579.1:p.Gln66Ter
NM_001350651.1:c.196C>T	NP_001337580.1:p.Gln66Ter
NR_146882.1:n.799C>T
NR_146883.1:n.613C>T
XM_011541497.3:c.601C>T	XP_011539799.1:p.Gln201Ter
XM_011541500.3:c.583C>T	XP_011539802.1:p.Gln195Ter
XM_011541501.2:c.583C>T	XP_011539803.1:p.Gln195Ter
XM_011541502.2:c.583C>T	XP_011539804.1:p.Gln195Ter
XM_011541503.2:c.583C>T	XP_011539805.1:p.Gln195Ter
XM_011541504.2:c.574C>T	XP_011539806.1:p.Gln192Ter
XM_011541505.2:c.163C>T	XP_011539807.1:p.Gln55Ter
XM_011541506.2:c.163C>T	XP_011539808.1:p.Gln55Ter
XM_017001331.1:c.583C>T	XP_016856820.1:p.Gln195Ter
XM_017001332.1:c.583C>T	XP_016856821.1:p.Gln195Ter
XM_017001333.1:c.583C>T	XP_016856822.1:p.Gln195Ter
XM_017001334.1:c.544C>T	XP_016856823.1:p.Gln182Ter
XM_017001335.1:c.265C>T	XP_016856824.1:p.Gln89Ter
XM_017001336.1:c.196C>T	XP_016856825.1:p.Gln66Ter
XM_017001337.1:c.196C>T	XP_016856826.1:p.Gln66Ter
XM_024447244.1:c.196C>T	XP_024303012.1:p.Gln66Ter
XM_024447245.1:c.196C>T	XP_024303013.1:p.Gln66Ter
XM_024447248.1:c.154C>T	XP_024303016.1:p.Gln52Ter
XM_024447249.1:c.25C>T	XP_024303017.1:p.Gln9Ter
XM_024447250.1:c.25C>T	XP_024303018.1:p.Gln9Ter
XM_024447251.1:c.25C>T	XP_024303019.1:p.Gln9Ter
XR_001737190.1:n.586C>T
XR_001737192.1:n.398C>T
XR_002956643.1:n.578C>T
XR_002956644.1:n.1113C>T
XR_946658.2:n.686C>T
NM_001048171.2:c.541C>T	NP_001041636.2:p.Gln181Ter
NM_001128425.2:c.625C>T MANE Plus Clinical	NP_001121897.1:p.Gln209Ter
NM_001048172.2:c.544C>T	NP_001041637.1:p.Gln182Ter
NM_001048173.2:c.541C>T	NP_001041638.1:p.Gln181Ter
NM_001048174.2:c.541C>T MANE Select	NP_001041639.1:p.Gln181Ter
NM_001293190.2:c.586C>T	NP_001280119.1:p.Gln196Ter
NM_001293191.2:c.574C>T	NP_001280120.1:p.Gln192Ter
NM_001293192.2:c.265C>T	NP_001280121.1:p.Gln89Ter
NM_001293195.2:c.541C>T	NP_001280124.1:p.Gln181Ter
NM_001293196.2:c.265C>T	NP_001280125.1:p.Gln89Ter
NM_001350650.2:c.196C>T	NP_001337579.1:p.Gln66Ter
NM_001350651.2:c.196C>T	NP_001337580.1:p.Gln66Ter
NM_012222.3:c.616C>T	NP_036354.1:p.Gln206Ter
NR_146882.2:n.769C>T
NR_146883.2:n.618C>T