Canonical Allele Identifier: CA2495832705

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412461_47412463delinsCTT , CM000664.2:g.47412461_47412463delinsCTT	GRCh38
NC_000002.11:g.47639600_47639602delinsCTT , CM000664.1:g.47639600_47639602delinsCTT	GRCh37
NC_000002.10:g.47493104_47493106delinsCTT	NCBI36
NG_007110.2:g.14338_14340delinsCTT , LRG_218:g.14338_14340delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.693_695delinsCTT	ENSP00000495641.2:p.Asp231=
ENST00000233146.7:c.693_695delinsCTT MANE Select	ENSP00000233146.2:p.Asp231=
ENST00000543555.6:c.495_497delinsCTT	ENSP00000442697.1:p.Asp165=
ENST00000644092.1:c.693_695delinsCTT	ENSP00000496351.1:p.Asp231=
ENST00000645339.1:c.693_695delinsCTT	ENSP00000496441.1:p.Asp231=
ENST00000645506.1:c.693_695delinsCTT	ENSP00000495455.1:p.Asp231=
ENST00000646415.1:c.693_695delinsCTT	ENSP00000495543.1:p.Asp231=
ENST00000233146.6:c.693_695delinsCTT	ENSP00000233146.2:p.Asp231=
ENST00000406134.5:c.693_695delinsCTT	ENSP00000384199.1:p.Asp231=
ENST00000543555.5:c.495_497delinsCTT	ENSP00000442697.1:p.Asp165=
ENST00000610696.4:c.693_695delinsCTT	ENSP00000483159.1:p.Asp231=
ENST00000613514.4:c.693_695delinsCTT	ENSP00000484137.1:p.Asp231=
ENST00000617333.3:c.693_695delinsCTT	ENSP00000482468.1:p.Asp231=
ENST00000617938.4:c.693_695delinsCTT	ENSP00000481158.1:p.Asp231=
ENST00000621359.2:c.693_695delinsCTT	ENSP00000481416.1:p.Asp231=
NM_000251.2:c.693_695delinsCTT , LRG_218t1:c.693_695delinsCTT	NP_000242.1:p.Asp231=
NM_001258281.1:c.495_497delinsCTT	NP_001245210.1:p.Asp165=
XM_005264332.2:c.693_695delinsCTT	XP_005264389.2:p.Asp231=
XM_011532867.1:c.693_695delinsCTT	XP_011531169.1:p.Asp231=
XR_939685.1:n.765_767delinsCTT
XM_005264332.4:c.693_695delinsCTT	XP_005264389.2:p.Asp231=
XM_011532867.2:c.693_695delinsCTT	XP_011531169.1:p.Asp231=
XR_001738747.2:n.755_757delinsCTT
XR_939685.2:n.755_757delinsCTT
NM_000251.3:c.693_695delinsCTT MANE Select	NP_000242.1:p.Asp231=