Canonical Allele Identifier: CA2473712271

Gene: MUTYH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331533A= , CM000663.2:g.45331533A=	GRCh38
NC_000001.10:g.45797205A= , CM000663.1:g.45797205A=	GRCh37
NC_000001.9:g.45569792A=	NCBI36
NG_008189.1:g.13938T= , LRG_220:g.13938T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.742T=	ENSP00000410263.2:p.Phe248=
ENST00000435155.2:c.1159T=	ENSP00000403655.2:p.Phe387=
ENST00000467459.6:c.1149T=	ENSP00000435889.2:p.Ser383=
ENST00000483127.2:c.1144T=	ENSP00000436469.2:p.Phe382=
ENST00000485271.6:c.1126T=	ENSP00000431264.2:p.Phe376=
ENST00000529892.6:c.979T=	ENSP00000432528.2:p.Phe327=
ENST00000533178.6:c.*455T=	ENSP00000436430.2:n.*455T=
ENST00000672314.2:c.1126T=	ENSP00000500828.2:p.Phe376=
ENST00000710952.2:c.1210T= MANE Plus Clinical	ENSP00000518552.2:p.Phe404=
ENST00000672818.3:c.1201T=	ENSP00000500891.1:p.Phe401=
ENST00000456914.7:c.1126T= MANE Select	ENSP00000407590.2:p.Phe376=
ENST00000671898.1:c.1714T=	ENSP00000499896.1:p.Phe572=
ENST00000672011.1:c.*455T=	ENSP00000500418.1:n.*455T=
ENST00000672314.1:c.1126T=	ENSP00000500828.1:p.Phe376=
ENST00000672593.1:c.*1352T=	ENSP00000500455.1:n.*1352T=
ENST00000672818.2:c.1201T=	ENSP00000500891.1:p.Phe401=
ENST00000673134.1:c.*823T=	ENSP00000500526.1:n.*823T=
ENST00000354383.10:c.1129T=	ENSP00000346354.6:p.Phe377=
ENST00000355498.6:c.1126T=	ENSP00000347685.2:p.Phe376=
ENST00000372098.7:c.1201T=	ENSP00000361170.3:p.Phe401=
ENST00000372104.5:c.1126T=	ENSP00000361176.1:p.Phe376=
ENST00000372110.7:c.1171T=	ENSP00000361182.3:p.Phe391=
ENST00000372115.7:c.1168T=	ENSP00000361187.3:p.Phe390=
ENST00000448481.5:c.1159T=	ENSP00000409718.1:p.Phe387=
ENST00000450313.5:c.1210T=	ENSP00000408176.1:p.Phe404=
ENST00000456914.6:c.1126T=	ENSP00000407590.2:p.Phe376=
ENST00000467459.5:c.543T=	ENSP00000435889.1:p.Ser181=
ENST00000475516.5:c.*939T=	ENSP00000433843.1:n.*939T=
ENST00000481571.5:c.*939T=	ENSP00000436597.1:n.*939T=
ENST00000482094.5:n.447T=
ENST00000488731.6:c.211T=	ENSP00000432330.1:p.Phe71=
ENST00000528013.6:c.1168T=	ENSP00000433130.2:p.Phe390=
ENST00000529892.5:c.201T=
ENST00000529984.5:c.211T=	ENSP00000437093.1:p.Phe71=
ENST00000531105.5:c.116-2096T=	ENSP00000431292.1:n.116-2096T=
ENST00000533178.5:c.755T=	ENSP00000436430.1:n.755T=
NM_001048171.1:c.1168T=	NP_001041636.1:p.Phe390=
NM_001048172.1:c.1129T=	NP_001041637.1:p.Phe377=
NM_001048173.1:c.1126T=	NP_001041638.1:p.Phe376=
NM_001048174.1:c.1126T=	NP_001041639.1:p.Phe376=
NM_001128425.1:c.1210T= , LRG_220t1:c.1210T=	NP_001121897.1:p.Phe404=
NM_001293190.1:c.1171T=	NP_001280119.1:p.Phe391=
NM_001293191.1:c.1159T=	NP_001280120.1:p.Phe387=
NM_001293192.1:c.850T=	NP_001280121.1:p.Phe284=
NM_001293195.1:c.1126T=	NP_001280124.1:p.Phe376=
NM_001293196.1:c.850T=	NP_001280125.1:p.Phe284=
NM_012222.2:c.1201T=	NP_036354.1:p.Phe401=
XM_011541497.1:c.1186T=	XP_011539799.1:p.Phe396=
XM_011541498.1:c.1168T=	XP_011539800.1:p.Phe390=
XM_011541499.1:c.1168T=	XP_011539801.1:p.Phe390=
XM_011541500.1:c.1168T=	XP_011539802.1:p.Phe390=
XM_011541501.1:c.1168T=	XP_011539803.1:p.Phe390=
XM_011541502.1:c.1168T=	XP_011539804.1:p.Phe390=
XM_011541503.1:c.1168T=	XP_011539805.1:p.Phe390=
XM_011541504.1:c.1159T=	XP_011539806.1:p.Phe387=
XM_011541505.1:c.748T=	XP_011539807.1:p.Phe250=
XM_011541506.1:c.748T=	XP_011539808.1:p.Phe250=
XM_011541507.1:c.739T=	XP_011539809.1:p.Phe247=
XM_011541508.1:c.754T=	XP_011539810.1:p.Phe252=
XR_946658.1:n.1257T=
NM_001350650.1:c.781T=	NP_001337579.1:p.Phe261=
NM_001350651.1:c.781T=	NP_001337580.1:p.Phe261=
NR_146882.1:n.1384T=
NR_146883.1:n.1198T=
XM_011541497.3:c.1186T=	XP_011539799.1:p.Phe396=
XM_011541500.3:c.1168T=	XP_011539802.1:p.Phe390=
XM_011541501.2:c.1168T=	XP_011539803.1:p.Phe390=
XM_011541502.2:c.1168T=	XP_011539804.1:p.Phe390=
XM_011541503.2:c.1168T=	XP_011539805.1:p.Phe390=
XM_011541504.2:c.1159T=	XP_011539806.1:p.Phe387=
XM_011541505.2:c.748T=	XP_011539807.1:p.Phe250=
XM_011541506.2:c.748T=	XP_011539808.1:p.Phe250=
XM_017001331.1:c.1168T=	XP_016856820.1:p.Phe390=
XM_017001332.1:c.1168T=	XP_016856821.1:p.Phe390=
XM_017001333.1:c.1168T=	XP_016856822.1:p.Phe390=
XM_017001334.1:c.1129T=	XP_016856823.1:p.Phe377=
XM_017001335.1:c.850T=	XP_016856824.1:p.Phe284=
XM_017001336.1:c.781T=	XP_016856825.1:p.Phe261=
XM_017001337.1:c.781T=	XP_016856826.1:p.Phe261=
XM_024447244.1:c.781T=	XP_024303012.1:p.Phe261=
XM_024447245.1:c.781T=	XP_024303013.1:p.Phe261=
XM_024447248.1:c.739T=	XP_024303016.1:p.Phe247=
XM_024447249.1:c.610T=	XP_024303017.1:p.Phe204=
XM_024447250.1:c.610T=	XP_024303018.1:p.Phe204=
XM_024447251.1:c.610T=	XP_024303019.1:p.Phe204=
XR_001737190.1:n.1171T=
XR_001737192.1:n.983T=
XR_002956643.1:n.1163T=
XR_002956644.1:n.1698T=
XR_946658.2:n.1271T=
NM_001048171.2:c.1126T=	NP_001041636.2:p.Phe376=
NM_001128425.2:c.1210T= MANE Plus Clinical	NP_001121897.1:p.Phe404=
NM_001048172.2:c.1129T=	NP_001041637.1:p.Phe377=
NM_001048173.2:c.1126T=	NP_001041638.1:p.Phe376=
NM_001048174.2:c.1126T= MANE Select	NP_001041639.1:p.Phe376=
NM_001293190.2:c.1171T=	NP_001280119.1:p.Phe391=
NM_001293191.2:c.1159T=	NP_001280120.1:p.Phe387=
NM_001293192.2:c.850T=	NP_001280121.1:p.Phe284=
NM_001293195.2:c.1126T=	NP_001280124.1:p.Phe376=
NM_001293196.2:c.850T=	NP_001280125.1:p.Phe284=
NM_001350650.2:c.781T=	NP_001337579.1:p.Phe261=
NM_001350651.2:c.781T=	NP_001337580.1:p.Phe261=
NM_012222.3:c.1201T=	NP_036354.1:p.Phe401=
NR_146882.2:n.1354T=
NR_146883.2:n.1203T=