Canonical Allele Identifier: CA2473712839

Gene: MUTYH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332652T= , CM000663.2:g.45332652T=	GRCh38
NC_000001.10:g.45798324T= , CM000663.1:g.45798324T=	GRCh37
NC_000001.9:g.45570911T=	NCBI36
NG_008189.1:g.12819A= , LRG_220:g.12819A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.144A=	ENSP00000410263.2:p.Thr48=
ENST00000435155.2:c.561A=	ENSP00000403655.2:p.Thr187=
ENST00000467459.6:c.528A=	ENSP00000435889.2:p.Thr176=
ENST00000483127.2:c.546A=	ENSP00000436469.2:p.Thr182=
ENST00000485271.6:c.528A=	ENSP00000431264.2:p.Thr176=
ENST00000529892.6:c.570A=	ENSP00000432528.2:p.Thr190=
ENST00000533178.6:c.151A=	ENSP00000436430.2:p.Ser51=
ENST00000672314.2:c.528A=	ENSP00000500828.2:p.Thr176=
ENST00000674679.2:c.*440A=	ENSP00000501623.2:n.*440A=
ENST00000710952.2:c.612A= MANE Plus Clinical	ENSP00000518552.2:p.Thr204=
ENST00000672818.3:c.603A=	ENSP00000500891.1:p.Thr201=
ENST00000450313.6:c.538A=	ENSP00000408176.2:p.Ser180=
ENST00000456914.7:c.528A= MANE Select	ENSP00000407590.2:p.Thr176=
ENST00000461495.6:c.*267A=	ENSP00000437166.1:n.*267A=
ENST00000671856.1:n.474A=
ENST00000671898.1:c.1116A=	ENSP00000499896.1:p.Thr372=
ENST00000672011.1:c.496A=	ENSP00000500418.1:p.Ser166=
ENST00000672314.1:c.528A=	ENSP00000500828.1:p.Thr176=
ENST00000672593.1:c.*416A=	ENSP00000500455.1:n.*416A=
ENST00000672764.1:c.487A=	ENSP00000500886.1:p.Ser163=
ENST00000672818.2:c.603A=	ENSP00000500891.1:p.Thr201=
ENST00000673134.1:c.*225A=	ENSP00000500526.1:n.*225A=
ENST00000674679.1:c.556A=	ENSP00000501623.1:n.556A=
ENST00000354383.10:c.531A=	ENSP00000346354.6:p.Thr177=
ENST00000355498.6:c.528A=	ENSP00000347685.2:p.Thr176=
ENST00000372098.7:c.603A=	ENSP00000361170.3:p.Thr201=
ENST00000372104.5:c.528A=	ENSP00000361176.1:p.Thr176=
ENST00000372110.7:c.573A=	ENSP00000361182.3:p.Thr191=
ENST00000372115.7:c.570A=	ENSP00000361187.3:p.Thr190=
ENST00000412971.5:c.144A=	ENSP00000410263.1:p.Thr48=
ENST00000435155.1:c.561A=	ENSP00000403655.1:p.Thr187=
ENST00000448481.5:c.561A=	ENSP00000409718.1:p.Thr187=
ENST00000450313.5:c.612A=	ENSP00000408176.1:p.Thr204=
ENST00000456914.6:c.528A=	ENSP00000407590.2:p.Thr176=
ENST00000461495.5:c.*267A=	ENSP00000437166.1:n.*267A=
ENST00000462388.5:n.219A=
ENST00000467940.5:c.*451A=	ENSP00000436478.1:n.*451A=
ENST00000470256.5:c.415A=	ENSP00000434985.1:p.Ser139=
ENST00000475516.5:c.*341A=	ENSP00000433843.1:n.*341A=
ENST00000478796.5:n.515A=
ENST00000479746.6:n.886A=
ENST00000481571.5:c.*341A=	ENSP00000436597.1:n.*341A=
ENST00000483642.5:n.1043A=
ENST00000488731.6:c.187+111A=	ENSP00000432330.1:n.187+111A=
ENST00000492494.5:n.925A=
ENST00000525160.5:c.*179A=	ENSP00000431568.1:n.*179A=
ENST00000528013.6:c.570A=	ENSP00000433130.2:p.Thr190=
ENST00000529984.5:c.187+111A=	ENSP00000437093.1:n.187+111A=
ENST00000531105.5:c.115+1739A=	ENSP00000431292.1:n.115+1739A=
ENST00000533178.5:c.157A=	ENSP00000436430.1:p.Ser53=
NM_001048171.1:c.570A=	NP_001041636.1:p.Thr190=
NM_001048172.1:c.531A=	NP_001041637.1:p.Thr177=
NM_001048173.1:c.528A=	NP_001041638.1:p.Thr176=
NM_001048174.1:c.528A=	NP_001041639.1:p.Thr176=
NM_001128425.1:c.612A= , LRG_220t1:c.612A=	NP_001121897.1:p.Thr204=
NM_001293190.1:c.573A=	NP_001280119.1:p.Thr191=
NM_001293191.1:c.561A=	NP_001280120.1:p.Thr187=
NM_001293192.1:c.252A=	NP_001280121.1:p.Thr84=
NM_001293195.1:c.528A=	NP_001280124.1:p.Thr176=
NM_001293196.1:c.252A=	NP_001280125.1:p.Thr84=
NM_012222.2:c.603A=	NP_036354.1:p.Thr201=
XM_011541497.1:c.588A=	XP_011539799.1:p.Thr196=
XM_011541498.1:c.570A=	XP_011539800.1:p.Thr190=
XM_011541499.1:c.570A=	XP_011539801.1:p.Thr190=
XM_011541500.1:c.570A=	XP_011539802.1:p.Thr190=
XM_011541501.1:c.570A=	XP_011539803.1:p.Thr190=
XM_011541502.1:c.570A=	XP_011539804.1:p.Thr190=
XM_011541503.1:c.570A=	XP_011539805.1:p.Thr190=
XM_011541504.1:c.561A=	XP_011539806.1:p.Thr187=
XM_011541505.1:c.150A=	XP_011539807.1:p.Thr50=
XM_011541506.1:c.150A=	XP_011539808.1:p.Thr50=
XM_011541507.1:c.141A=	XP_011539809.1:p.Thr47=
XM_011541508.1:c.156A=	XP_011539810.1:p.Thr52=
XR_946658.1:n.659A=
NM_001350650.1:c.183A=	NP_001337579.1:p.Thr61=
NM_001350651.1:c.183A=	NP_001337580.1:p.Thr61=
NR_146882.1:n.786A=
NR_146883.1:n.600A=
XM_011541497.3:c.588A=	XP_011539799.1:p.Thr196=
XM_011541500.3:c.570A=	XP_011539802.1:p.Thr190=
XM_011541501.2:c.570A=	XP_011539803.1:p.Thr190=
XM_011541502.2:c.570A=	XP_011539804.1:p.Thr190=
XM_011541503.2:c.570A=	XP_011539805.1:p.Thr190=
XM_011541504.2:c.561A=	XP_011539806.1:p.Thr187=
XM_011541505.2:c.150A=	XP_011539807.1:p.Thr50=
XM_011541506.2:c.150A=	XP_011539808.1:p.Thr50=
XM_017001331.1:c.570A=	XP_016856820.1:p.Thr190=
XM_017001332.1:c.570A=	XP_016856821.1:p.Thr190=
XM_017001333.1:c.570A=	XP_016856822.1:p.Thr190=
XM_017001334.1:c.531A=	XP_016856823.1:p.Thr177=
XM_017001335.1:c.252A=	XP_016856824.1:p.Thr84=
XM_017001336.1:c.183A=	XP_016856825.1:p.Thr61=
XM_017001337.1:c.183A=	XP_016856826.1:p.Thr61=
XM_024447244.1:c.183A=	XP_024303012.1:p.Thr61=
XM_024447245.1:c.183A=	XP_024303013.1:p.Thr61=
XM_024447248.1:c.141A=	XP_024303016.1:p.Thr47=
XM_024447249.1:c.12A=	XP_024303017.1:p.Thr4=
XM_024447250.1:c.12A=	XP_024303018.1:p.Thr4=
XM_024447251.1:c.12A=	XP_024303019.1:p.Thr4=
XR_001737190.1:n.573A=
XR_001737192.1:n.385A=
XR_002956643.1:n.565A=
XR_002956644.1:n.1100A=
XR_946658.2:n.673A=
NM_001048171.2:c.528A=	NP_001041636.2:p.Thr176=
NM_001128425.2:c.612A= MANE Plus Clinical	NP_001121897.1:p.Thr204=
NM_001048172.2:c.531A=	NP_001041637.1:p.Thr177=
NM_001048173.2:c.528A=	NP_001041638.1:p.Thr176=
NM_001048174.2:c.528A= MANE Select	NP_001041639.1:p.Thr176=
NM_001293190.2:c.573A=	NP_001280119.1:p.Thr191=
NM_001293191.2:c.561A=	NP_001280120.1:p.Thr187=
NM_001293192.2:c.252A=	NP_001280121.1:p.Thr84=
NM_001293195.2:c.528A=	NP_001280124.1:p.Thr176=
NM_001293196.2:c.252A=	NP_001280125.1:p.Thr84=
NM_001350650.2:c.183A=	NP_001337579.1:p.Thr61=
NM_001350651.2:c.183A=	NP_001337580.1:p.Thr61=
NM_012222.3:c.603A=	NP_036354.1:p.Thr201=
NR_146882.2:n.756A=
NR_146883.2:n.605A=