Canonical Allele Identifier: CA019004

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47470989G>C , CM000664.2:g.47470989G>C	GRCh38
NC_000002.11:g.47698128G>C , CM000664.1:g.47698128G>C	GRCh37
NC_000002.10:g.47551632G>C	NCBI36
NG_007110.2:g.72866G>C , LRG_218:g.72866G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000251.3:c.1686G>C MANE Select	NP_000242.1:p.Glu562Asp
ENST00000233146.7:c.1686G>C MANE Select	ENSP00000233146.2:p.Glu562Asp
NM_000251.2:c.1686G>C , LRG_218t1:c.1686G>C	NP_000242.1:p.Glu562Asp
NM_001258281.1:c.1488G>C	NP_001245210.1:p.Glu496Asp
ENST00000233146.6:c.1686G>C	ENSP00000233146.2:p.Glu562Asp
ENST00000406134.5:c.1686G>C	ENSP00000384199.1:p.Glu562Asp
ENST00000543555.5:c.1488G>C	ENSP00000442697.1:p.Glu496Asp
ENST00000543555.6:c.1488G>C	ENSP00000442697.1:p.Glu496Asp
ENST00000610696.4:c.*82G>C	ENSP00000483159.1:n.*82G>C
ENST00000613514.4:c.*226G>C	ENSP00000484137.1:n.*226G>C
ENST00000617333.3:c.*452G>C	ENSP00000482468.1:n.*452G>C
ENST00000617938.4:c.*658G>C	ENSP00000481158.1:n.*658G>C
ENST00000621359.2:c.1686G>C	ENSP00000481416.1:p.Glu562Asp
ENST00000644092.1:c.1663G>C	ENSP00000496351.1:p.Val555Leu
ENST00000644900.2:c.1686G>C	ENSP00000495641.2:p.Glu562Asp
ENST00000645339.1:c.1686G>C	ENSP00000496441.1:p.Glu562Asp
ENST00000645506.1:c.1686G>C	ENSP00000495455.1:p.Glu562Asp
ENST00000646415.1:c.1686G>C	ENSP00000495543.1:p.Glu562Asp
XM_005264332.2:c.1686G>C	XP_005264389.2:p.Glu562Asp
XM_005264332.4:c.1686G>C	XP_005264389.2:p.Glu562Asp
XM_011532867.1:c.1686G>C	XP_011531169.1:p.Glu562Asp
XM_011532867.2:c.1686G>C	XP_011531169.1:p.Glu562Asp
XR_001738747.2:n.1748G>C
XR_939685.1:n.1758G>C
XR_939685.2:n.1748G>C