Canonical Allele Identifier: CA340135576

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45798447C>T (hg19) ; chr1:g.45332775C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332775C>T , CM000663.2:g.45332775C>T	GRCh38
NC_000001.10:g.45798447C>T , CM000663.1:g.45798447C>T	GRCh37
NC_000001.9:g.45571034C>T	NCBI36
NG_008189.1:g.12696G>A , LRG_220:g.12696G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.96G>A	ENSP00000410263.2:p.Glu32=
ENST00000435155.2:c.513G>A	ENSP00000403655.2:p.Glu171=
ENST00000467459.6:c.480G>A	ENSP00000435889.2:p.Glu160=
ENST00000483127.2:c.498G>A	ENSP00000436469.2:p.Glu166=
ENST00000485271.6:c.480G>A	ENSP00000431264.2:p.Glu160=
ENST00000529892.6:c.522G>A	ENSP00000432528.2:p.Glu174=
ENST00000533178.6:c.116-88G>A	ENSP00000436430.2:n.116-88G>A
ENST00000672314.2:c.480G>A	ENSP00000500828.2:p.Glu160=
ENST00000674679.2:c.*392G>A	ENSP00000501623.2:n.*392G>A
ENST00000710952.2:c.564G>A MANE Plus Clinical	ENSP00000518552.2:p.Glu188=
ENST00000672818.3:c.555G>A	ENSP00000500891.1:p.Glu185=
ENST00000450313.6:c.490G>A	ENSP00000408176.2:p.Gly164Arg
ENST00000456914.7:c.480G>A MANE Select	ENSP00000407590.2:p.Glu160=
ENST00000461495.6:c.*219G>A	ENSP00000437166.1:n.*219G>A
ENST00000671856.1:n.426G>A
ENST00000671898.1:c.1068G>A	ENSP00000499896.1:p.Glu356=
ENST00000672011.1:c.448G>A	ENSP00000500418.1:p.Gly150Arg
ENST00000672314.1:c.480G>A	ENSP00000500828.1:p.Glu160=
ENST00000672593.1:c.*293G>A	ENSP00000500455.1:n.*293G>A
ENST00000672764.1:c.439G>A	ENSP00000500886.1:p.Gly147Arg
ENST00000672818.2:c.555G>A	ENSP00000500891.1:p.Glu185=
ENST00000673134.1:c.*177G>A	ENSP00000500526.1:n.*177G>A
ENST00000674679.1:c.508G>A	ENSP00000501623.1:n.508G>A
ENST00000354383.10:c.483G>A	ENSP00000346354.6:p.Glu161=
ENST00000355498.6:c.480G>A	ENSP00000347685.2:p.Glu160=
ENST00000372098.7:c.555G>A	ENSP00000361170.3:p.Glu185=
ENST00000372104.5:c.480G>A	ENSP00000361176.1:p.Glu160=
ENST00000372110.7:c.525G>A	ENSP00000361182.3:p.Glu175=
ENST00000372115.7:c.522G>A	ENSP00000361187.3:p.Glu174=
ENST00000412971.5:c.96G>A	ENSP00000410263.1:p.Glu32=
ENST00000435155.1:c.513G>A	ENSP00000403655.1:p.Glu171=
ENST00000448481.5:c.513G>A	ENSP00000409718.1:p.Glu171=
ENST00000450313.5:c.564G>A	ENSP00000408176.1:p.Glu188=
ENST00000456914.6:c.480G>A	ENSP00000407590.2:p.Glu160=
ENST00000461495.5:c.*219G>A	ENSP00000437166.1:n.*219G>A
ENST00000462388.5:n.171G>A
ENST00000467940.5:c.*403G>A	ENSP00000436478.1:n.*403G>A
ENST00000470256.5:c.367G>A	ENSP00000434985.1:p.Gly123Arg
ENST00000475516.5:c.*293G>A	ENSP00000433843.1:n.*293G>A
ENST00000476789.5:n.920G>A
ENST00000478796.5:n.467G>A
ENST00000479746.6:n.763G>A
ENST00000481139.5:n.953G>A
ENST00000481571.5:c.*293G>A	ENSP00000436597.1:n.*293G>A
ENST00000483642.5:n.995G>A
ENST00000485484.5:n.781G>A
ENST00000488731.6:c.175G>A	ENSP00000432330.1:p.Gly59Arg
ENST00000492494.5:n.877G>A
ENST00000525160.5:c.*131G>A	ENSP00000431568.1:n.*131G>A
ENST00000528013.6:c.522G>A	ENSP00000433130.2:p.Glu174=
ENST00000529984.5:c.175G>A	ENSP00000437093.1:p.Gly59Arg
ENST00000531105.5:c.115+1616G>A	ENSP00000431292.1:n.115+1616G>A
ENST00000533178.5:c.122-88G>A	ENSP00000436430.1:n.122-88G>A
NM_001048171.1:c.522G>A	NP_001041636.1:p.Glu174=
NM_001048172.1:c.483G>A	NP_001041637.1:p.Glu161=
NM_001048173.1:c.480G>A	NP_001041638.1:p.Glu160=
NM_001048174.1:c.480G>A	NP_001041639.1:p.Glu160=
NM_001128425.1:c.564G>A , LRG_220t1:c.564G>A	NP_001121897.1:p.Glu188=
NM_001293190.1:c.525G>A	NP_001280119.1:p.Glu175=
NM_001293191.1:c.513G>A	NP_001280120.1:p.Glu171=
NM_001293192.1:c.204G>A	NP_001280121.1:p.Glu68=
NM_001293195.1:c.480G>A	NP_001280124.1:p.Glu160=
NM_001293196.1:c.204G>A	NP_001280125.1:p.Glu68=
NM_012222.2:c.555G>A	NP_036354.1:p.Glu185=
XM_011541497.1:c.540G>A	XP_011539799.1:p.Glu180=
XM_011541498.1:c.522G>A	XP_011539800.1:p.Glu174=
XM_011541499.1:c.522G>A	XP_011539801.1:p.Glu174=
XM_011541500.1:c.522G>A	XP_011539802.1:p.Glu174=
XM_011541501.1:c.522G>A	XP_011539803.1:p.Glu174=
XM_011541502.1:c.522G>A	XP_011539804.1:p.Glu174=
XM_011541503.1:c.522G>A	XP_011539805.1:p.Glu174=
XM_011541504.1:c.513G>A	XP_011539806.1:p.Glu171=
XM_011541505.1:c.102G>A	XP_011539807.1:p.Glu34=
XM_011541506.1:c.102G>A	XP_011539808.1:p.Glu34=
XM_011541507.1:c.93G>A	XP_011539809.1:p.Glu31=
XM_011541508.1:c.108G>A	XP_011539810.1:p.Glu36=
XR_946658.1:n.611G>A
NM_001350650.1:c.135G>A	NP_001337579.1:p.Glu45=
NM_001350651.1:c.135G>A	NP_001337580.1:p.Glu45=
NR_146882.1:n.738G>A
NR_146883.1:n.552G>A
XM_011541497.3:c.540G>A	XP_011539799.1:p.Glu180=
XM_011541500.3:c.522G>A	XP_011539802.1:p.Glu174=
XM_011541501.2:c.522G>A	XP_011539803.1:p.Glu174=
XM_011541502.2:c.522G>A	XP_011539804.1:p.Glu174=
XM_011541503.2:c.522G>A	XP_011539805.1:p.Glu174=
XM_011541504.2:c.513G>A	XP_011539806.1:p.Glu171=
XM_011541505.2:c.102G>A	XP_011539807.1:p.Glu34=
XM_011541506.2:c.102G>A	XP_011539808.1:p.Glu34=
XM_017001331.1:c.522G>A	XP_016856820.1:p.Glu174=
XM_017001332.1:c.522G>A	XP_016856821.1:p.Glu174=
XM_017001333.1:c.522G>A	XP_016856822.1:p.Glu174=
XM_017001334.1:c.483G>A	XP_016856823.1:p.Glu161=
XM_017001335.1:c.204G>A	XP_016856824.1:p.Glu68=
XM_017001336.1:c.135G>A	XP_016856825.1:p.Glu45=
XM_017001337.1:c.135G>A	XP_016856826.1:p.Glu45=
XM_024447244.1:c.135G>A	XP_024303012.1:p.Glu45=
XM_024447245.1:c.135G>A	XP_024303013.1:p.Glu45=
XM_024447248.1:c.93G>A	XP_024303016.1:p.Glu31=
XM_024447249.1:c.-37G>A	XP_024303017.1:n.-37G>A
XM_024447250.1:c.-37G>A	XP_024303018.1:n.-37G>A
XM_024447251.1:c.-37G>A	XP_024303019.1:n.-37G>A
XR_001737190.1:n.525G>A
XR_001737192.1:n.337G>A
XR_002956643.1:n.517G>A
XR_002956644.1:n.1052G>A
XR_946658.2:n.625G>A
NM_001048171.2:c.480G>A	NP_001041636.2:p.Glu160=
NM_001128425.2:c.564G>A MANE Plus Clinical	NP_001121897.1:p.Glu188=
NM_001048172.2:c.483G>A	NP_001041637.1:p.Glu161=
NM_001048173.2:c.480G>A	NP_001041638.1:p.Glu160=
NM_001048174.2:c.480G>A MANE Select	NP_001041639.1:p.Glu160=
NM_001293190.2:c.525G>A	NP_001280119.1:p.Glu175=
NM_001293191.2:c.513G>A	NP_001280120.1:p.Glu171=
NM_001293192.2:c.204G>A	NP_001280121.1:p.Glu68=
NM_001293195.2:c.480G>A	NP_001280124.1:p.Glu160=
NM_001293196.2:c.204G>A	NP_001280125.1:p.Glu68=
NM_001350650.2:c.135G>A	NP_001337579.1:p.Glu45=
NM_001350651.2:c.135G>A	NP_001337580.1:p.Glu45=
NM_012222.3:c.555G>A	NP_036354.1:p.Glu185=
NR_146882.2:n.708G>A
NR_146883.2:n.557G>A