Canonical Allele Identifier: CA340132996

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45797177T>A (hg19) ; chr1:g.45331505T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331505T>A , CM000663.2:g.45331505T>A	GRCh38
NC_000001.10:g.45797177T>A , CM000663.1:g.45797177T>A	GRCh37
NC_000001.9:g.45569764T>A	NCBI36
NG_008189.1:g.13966A>T , LRG_220:g.13966A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.770A>T	ENSP00000410263.2:p.Glu257Val
ENST00000435155.2:c.1187A>T	ENSP00000403655.2:p.Glu396Val
ENST00000467459.6:c.*16A>T	ENSP00000435889.2:n.*16A>T
ENST00000483127.2:c.1172A>T	ENSP00000436469.2:p.Glu391Val
ENST00000485271.6:c.1154A>T	ENSP00000431264.2:p.Glu385Val
ENST00000529892.6:c.1007A>T	ENSP00000432528.2:p.Glu336Val
ENST00000533178.6:c.*483A>T	ENSP00000436430.2:n.*483A>T
ENST00000672314.2:c.1154A>T	ENSP00000500828.2:p.Glu385Val
ENST00000710952.2:c.1238A>T MANE Plus Clinical	ENSP00000518552.2:p.Glu413Val
ENST00000672818.3:c.1229A>T	ENSP00000500891.1:p.Glu410Val
ENST00000456914.7:c.1154A>T MANE Select	ENSP00000407590.2:p.Glu385Val
ENST00000671898.1:c.1742A>T	ENSP00000499896.1:p.Glu581Val
ENST00000672011.1:c.*483A>T	ENSP00000500418.1:n.*483A>T
ENST00000672314.1:c.1154A>T	ENSP00000500828.1:p.Glu385Val
ENST00000672593.1:c.*1380A>T	ENSP00000500455.1:n.*1380A>T
ENST00000672818.2:c.1229A>T	ENSP00000500891.1:p.Glu410Val
ENST00000673134.1:c.*851A>T	ENSP00000500526.1:n.*851A>T
ENST00000354383.10:c.1157A>T	ENSP00000346354.6:p.Glu386Val
ENST00000355498.6:c.1154A>T	ENSP00000347685.2:p.Glu385Val
ENST00000372098.7:c.1229A>T	ENSP00000361170.3:p.Glu410Val
ENST00000372104.5:c.1154A>T	ENSP00000361176.1:p.Glu385Val
ENST00000372110.7:c.1199A>T	ENSP00000361182.3:p.Glu400Val
ENST00000372115.7:c.1196A>T	ENSP00000361187.3:p.Glu399Val
ENST00000448481.5:c.1187A>T	ENSP00000409718.1:p.Glu396Val
ENST00000450313.5:c.1238A>T	ENSP00000408176.1:p.Glu413Val
ENST00000456914.6:c.1154A>T	ENSP00000407590.2:p.Glu385Val
ENST00000467459.5:c.571A>T	ENSP00000435889.1:n.571A>T
ENST00000475516.5:c.*967A>T	ENSP00000433843.1:n.*967A>T
ENST00000481571.5:c.*967A>T	ENSP00000436597.1:n.*967A>T
ENST00000482094.5:n.475A>T
ENST00000488731.6:c.239A>T	ENSP00000432330.1:p.Glu80Val
ENST00000528013.6:c.1196A>T	ENSP00000433130.2:p.Glu399Val
ENST00000529892.5:c.229A>T
ENST00000529984.5:c.239A>T	ENSP00000437093.1:p.Glu80Val
ENST00000531105.5:c.116-2068A>T	ENSP00000431292.1:n.116-2068A>T
ENST00000533178.5:c.783A>T	ENSP00000436430.1:n.783A>T
NM_001048171.1:c.1196A>T	NP_001041636.1:p.Glu399Val
NM_001048172.1:c.1157A>T	NP_001041637.1:p.Glu386Val
NM_001048173.1:c.1154A>T	NP_001041638.1:p.Glu385Val
NM_001048174.1:c.1154A>T	NP_001041639.1:p.Glu385Val
NM_001128425.1:c.1238A>T , LRG_220t1:c.1238A>T	NP_001121897.1:p.Glu413Val
NM_001293190.1:c.1199A>T	NP_001280119.1:p.Glu400Val
NM_001293191.1:c.1187A>T	NP_001280120.1:p.Glu396Val
NM_001293192.1:c.878A>T	NP_001280121.1:p.Glu293Val
NM_001293195.1:c.1154A>T	NP_001280124.1:p.Glu385Val
NM_001293196.1:c.878A>T	NP_001280125.1:p.Glu293Val
NM_012222.2:c.1229A>T	NP_036354.1:p.Glu410Val
XM_011541497.1:c.1214A>T	XP_011539799.1:p.Glu405Val
XM_011541498.1:c.1196A>T	XP_011539800.1:p.Glu399Val
XM_011541499.1:c.1196A>T	XP_011539801.1:p.Glu399Val
XM_011541500.1:c.1196A>T	XP_011539802.1:p.Glu399Val
XM_011541501.1:c.1196A>T	XP_011539803.1:p.Glu399Val
XM_011541502.1:c.1196A>T	XP_011539804.1:p.Glu399Val
XM_011541503.1:c.1196A>T	XP_011539805.1:p.Glu399Val
XM_011541504.1:c.1187A>T	XP_011539806.1:p.Glu396Val
XM_011541505.1:c.776A>T	XP_011539807.1:p.Glu259Val
XM_011541506.1:c.776A>T	XP_011539808.1:p.Glu259Val
XM_011541507.1:c.767A>T	XP_011539809.1:p.Glu256Val
XM_011541508.1:c.782A>T	XP_011539810.1:p.Glu261Val
XR_946658.1:n.1285A>T
NM_001350650.1:c.809A>T	NP_001337579.1:p.Glu270Val
NM_001350651.1:c.809A>T	NP_001337580.1:p.Glu270Val
NR_146882.1:n.1412A>T
NR_146883.1:n.1226A>T
XM_011541497.3:c.1214A>T	XP_011539799.1:p.Glu405Val
XM_011541500.3:c.1196A>T	XP_011539802.1:p.Glu399Val
XM_011541501.2:c.1196A>T	XP_011539803.1:p.Glu399Val
XM_011541502.2:c.1196A>T	XP_011539804.1:p.Glu399Val
XM_011541503.2:c.1196A>T	XP_011539805.1:p.Glu399Val
XM_011541504.2:c.1187A>T	XP_011539806.1:p.Glu396Val
XM_011541505.2:c.776A>T	XP_011539807.1:p.Glu259Val
XM_011541506.2:c.776A>T	XP_011539808.1:p.Glu259Val
XM_017001331.1:c.1196A>T	XP_016856820.1:p.Glu399Val
XM_017001332.1:c.1196A>T	XP_016856821.1:p.Glu399Val
XM_017001333.1:c.1196A>T	XP_016856822.1:p.Glu399Val
XM_017001334.1:c.1157A>T	XP_016856823.1:p.Glu386Val
XM_017001335.1:c.878A>T	XP_016856824.1:p.Glu293Val
XM_017001336.1:c.809A>T	XP_016856825.1:p.Glu270Val
XM_017001337.1:c.809A>T	XP_016856826.1:p.Glu270Val
XM_024447244.1:c.809A>T	XP_024303012.1:p.Glu270Val
XM_024447245.1:c.809A>T	XP_024303013.1:p.Glu270Val
XM_024447248.1:c.767A>T	XP_024303016.1:p.Glu256Val
XM_024447249.1:c.638A>T	XP_024303017.1:p.Glu213Val
XM_024447250.1:c.638A>T	XP_024303018.1:p.Glu213Val
XM_024447251.1:c.638A>T	XP_024303019.1:p.Glu213Val
XR_001737190.1:n.1199A>T
XR_001737192.1:n.1011A>T
XR_002956643.1:n.1191A>T
XR_002956644.1:n.1726A>T
XR_946658.2:n.1299A>T
NM_001048171.2:c.1154A>T	NP_001041636.2:p.Glu385Val
NM_001128425.2:c.1238A>T MANE Plus Clinical	NP_001121897.1:p.Glu413Val
NM_001048172.2:c.1157A>T	NP_001041637.1:p.Glu386Val
NM_001048173.2:c.1154A>T	NP_001041638.1:p.Glu385Val
NM_001048174.2:c.1154A>T MANE Select	NP_001041639.1:p.Glu385Val
NM_001293190.2:c.1199A>T	NP_001280119.1:p.Glu400Val
NM_001293191.2:c.1187A>T	NP_001280120.1:p.Glu396Val
NM_001293192.2:c.878A>T	NP_001280121.1:p.Glu293Val
NM_001293195.2:c.1154A>T	NP_001280124.1:p.Glu385Val
NM_001293196.2:c.878A>T	NP_001280125.1:p.Glu293Val
NM_001350650.2:c.809A>T	NP_001337579.1:p.Glu270Val
NM_001350651.2:c.809A>T	NP_001337580.1:p.Glu270Val
NM_012222.3:c.1229A>T	NP_036354.1:p.Glu410Val
NR_146882.2:n.1382A>T
NR_146883.2:n.1231A>T