Canonical Allele Identifier: CA340135438
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 926550
dbSNP Id: rs1645156886
gnomAD v4: 1-45332671-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332671C>T , CM000663.2:g.45332671C>T GRCh38
NC_000001.10:g.45798343C>T , CM000663.1:g.45798343C>T GRCh37
NC_000001.9:g.45570930C>T NCBI36
NG_008189.1:g.12800G>A , LRG_220:g.12800G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.125G>A ENSP00000410263.2:p.Gly42Glu
ENST00000435155.2:c.542G>A ENSP00000403655.2:p.Gly181Glu
ENST00000467459.6:c.509G>A ENSP00000435889.2:p.Gly170Glu
ENST00000483127.2:c.527G>A ENSP00000436469.2:p.Gly176Glu
ENST00000485271.6:c.509G>A ENSP00000431264.2:p.Gly170Glu
ENST00000529892.6:c.551G>A ENSP00000432528.2:p.Gly184Glu
ENST00000533178.6:c.132G>A ENSP00000436430.2:p.Arg44=
ENST00000672314.2:c.509G>A ENSP00000500828.2:p.Gly170Glu
ENST00000674679.2:c.*421G>A ENSP00000501623.2:n.*421G>A
ENST00000710952.2:c.593G>A MANE Plus Clinical ENSP00000518552.2:p.Gly198Glu
ENST00000672818.3:c.584G>A ENSP00000500891.1:p.Gly195Glu
ENST00000450313.6:c.519G>A ENSP00000408176.2:p.Arg173=
ENST00000456914.7:c.509G>A MANE Select ENSP00000407590.2:p.Gly170Glu
ENST00000461495.6:c.*248G>A ENSP00000437166.1:n.*248G>A
ENST00000671856.1:n.455G>A
ENST00000671898.1:c.1097G>A ENSP00000499896.1:p.Gly366Glu
ENST00000672011.1:c.477G>A ENSP00000500418.1:p.Arg159=
ENST00000672314.1:c.509G>A ENSP00000500828.1:p.Gly170Glu
ENST00000672593.1:c.*397G>A ENSP00000500455.1:n.*397G>A
ENST00000672764.1:c.468G>A ENSP00000500886.1:p.Arg156=
ENST00000672818.2:c.584G>A ENSP00000500891.1:p.Gly195Glu
ENST00000673134.1:c.*206G>A ENSP00000500526.1:n.*206G>A
ENST00000674679.1:c.537G>A ENSP00000501623.1:n.537G>A
ENST00000354383.10:c.512G>A ENSP00000346354.6:p.Gly171Glu
ENST00000355498.6:c.509G>A ENSP00000347685.2:p.Gly170Glu
ENST00000372098.7:c.584G>A ENSP00000361170.3:p.Gly195Glu
ENST00000372104.5:c.509G>A ENSP00000361176.1:p.Gly170Glu
ENST00000372110.7:c.554G>A ENSP00000361182.3:p.Gly185Glu
ENST00000372115.7:c.551G>A ENSP00000361187.3:p.Gly184Glu
ENST00000412971.5:c.125G>A ENSP00000410263.1:p.Gly42Glu
ENST00000435155.1:c.542G>A ENSP00000403655.1:p.Gly181Glu
ENST00000448481.5:c.542G>A ENSP00000409718.1:p.Gly181Glu
ENST00000450313.5:c.593G>A ENSP00000408176.1:p.Gly198Glu
ENST00000456914.6:c.509G>A ENSP00000407590.2:p.Gly170Glu
ENST00000461495.5:c.*248G>A ENSP00000437166.1:n.*248G>A
ENST00000462388.5:n.200G>A
ENST00000467940.5:c.*432G>A ENSP00000436478.1:n.*432G>A
ENST00000470256.5:c.396G>A ENSP00000434985.1:p.Arg132=
ENST00000475516.5:c.*322G>A ENSP00000433843.1:n.*322G>A
ENST00000478796.5:n.496G>A
ENST00000479746.6:n.867G>A
ENST00000481571.5:c.*322G>A ENSP00000436597.1:n.*322G>A
ENST00000483642.5:n.1024G>A
ENST00000488731.6:c.187+92G>A ENSP00000432330.1:n.187+92G>A
ENST00000492494.5:n.906G>A
ENST00000525160.5:c.*160G>A ENSP00000431568.1:n.*160G>A
ENST00000528013.6:c.551G>A ENSP00000433130.2:p.Gly184Glu
ENST00000529984.5:c.187+92G>A ENSP00000437093.1:n.187+92G>A
ENST00000531105.5:c.115+1720G>A ENSP00000431292.1:n.115+1720G>A
ENST00000533178.5:c.138G>A ENSP00000436430.1:p.Arg46=
NM_001048171.1:c.551G>A NP_001041636.1:p.Gly184Glu
NM_001048172.1:c.512G>A NP_001041637.1:p.Gly171Glu
NM_001048173.1:c.509G>A NP_001041638.1:p.Gly170Glu
NM_001048174.1:c.509G>A NP_001041639.1:p.Gly170Glu
NM_001128425.1:c.593G>A , LRG_220t1:c.593G>A NP_001121897.1:p.Gly198Glu
NM_001293190.1:c.554G>A NP_001280119.1:p.Gly185Glu
NM_001293191.1:c.542G>A NP_001280120.1:p.Gly181Glu
NM_001293192.1:c.233G>A NP_001280121.1:p.Gly78Glu
NM_001293195.1:c.509G>A NP_001280124.1:p.Gly170Glu
NM_001293196.1:c.233G>A NP_001280125.1:p.Gly78Glu
NM_012222.2:c.584G>A NP_036354.1:p.Gly195Glu
XM_011541497.1:c.569G>A XP_011539799.1:p.Gly190Glu
XM_011541498.1:c.551G>A XP_011539800.1:p.Gly184Glu
XM_011541499.1:c.551G>A XP_011539801.1:p.Gly184Glu
XM_011541500.1:c.551G>A XP_011539802.1:p.Gly184Glu
XM_011541501.1:c.551G>A XP_011539803.1:p.Gly184Glu
XM_011541502.1:c.551G>A XP_011539804.1:p.Gly184Glu
XM_011541503.1:c.551G>A XP_011539805.1:p.Gly184Glu
XM_011541504.1:c.542G>A XP_011539806.1:p.Gly181Glu
XM_011541505.1:c.131G>A XP_011539807.1:p.Gly44Glu
XM_011541506.1:c.131G>A XP_011539808.1:p.Gly44Glu
XM_011541507.1:c.122G>A XP_011539809.1:p.Gly41Glu
XM_011541508.1:c.137G>A XP_011539810.1:p.Gly46Glu
XR_946658.1:n.640G>A
NM_001350650.1:c.164G>A NP_001337579.1:p.Gly55Glu
NM_001350651.1:c.164G>A NP_001337580.1:p.Gly55Glu
NR_146882.1:n.767G>A
NR_146883.1:n.581G>A
XM_011541497.3:c.569G>A XP_011539799.1:p.Gly190Glu
XM_011541500.3:c.551G>A XP_011539802.1:p.Gly184Glu
XM_011541501.2:c.551G>A XP_011539803.1:p.Gly184Glu
XM_011541502.2:c.551G>A XP_011539804.1:p.Gly184Glu
XM_011541503.2:c.551G>A XP_011539805.1:p.Gly184Glu
XM_011541504.2:c.542G>A XP_011539806.1:p.Gly181Glu
XM_011541505.2:c.131G>A XP_011539807.1:p.Gly44Glu
XM_011541506.2:c.131G>A XP_011539808.1:p.Gly44Glu
XM_017001331.1:c.551G>A XP_016856820.1:p.Gly184Glu
XM_017001332.1:c.551G>A XP_016856821.1:p.Gly184Glu
XM_017001333.1:c.551G>A XP_016856822.1:p.Gly184Glu
XM_017001334.1:c.512G>A XP_016856823.1:p.Gly171Glu
XM_017001335.1:c.233G>A XP_016856824.1:p.Gly78Glu
XM_017001336.1:c.164G>A XP_016856825.1:p.Gly55Glu
XM_017001337.1:c.164G>A XP_016856826.1:p.Gly55Glu
XM_024447244.1:c.164G>A XP_024303012.1:p.Gly55Glu
XM_024447245.1:c.164G>A XP_024303013.1:p.Gly55Glu
XM_024447248.1:c.122G>A XP_024303016.1:p.Gly41Glu
XM_024447249.1:c.-8G>A XP_024303017.1:n.-8G>A
XM_024447250.1:c.-8G>A XP_024303018.1:n.-8G>A
XM_024447251.1:c.-8G>A XP_024303019.1:n.-8G>A
XR_001737190.1:n.554G>A
XR_001737192.1:n.366G>A
XR_002956643.1:n.546G>A
XR_002956644.1:n.1081G>A
XR_946658.2:n.654G>A
NM_001048171.2:c.509G>A NP_001041636.2:p.Gly170Glu
NM_001128425.2:c.593G>A MANE Plus Clinical NP_001121897.1:p.Gly198Glu
NM_001048172.2:c.512G>A NP_001041637.1:p.Gly171Glu
NM_001048173.2:c.509G>A NP_001041638.1:p.Gly170Glu
NM_001048174.2:c.509G>A MANE Select NP_001041639.1:p.Gly170Glu
NM_001293190.2:c.554G>A NP_001280119.1:p.Gly185Glu
NM_001293191.2:c.542G>A NP_001280120.1:p.Gly181Glu
NM_001293192.2:c.233G>A NP_001280121.1:p.Gly78Glu
NM_001293195.2:c.509G>A NP_001280124.1:p.Gly170Glu
NM_001293196.2:c.233G>A NP_001280125.1:p.Gly78Glu
NM_001350650.2:c.164G>A NP_001337579.1:p.Gly55Glu
NM_001350651.2:c.164G>A NP_001337580.1:p.Gly55Glu
NM_012222.3:c.584G>A NP_036354.1:p.Gly195Glu
NR_146882.2:n.737G>A
NR_146883.2:n.586G>A