Canonical Allele Identifier: CA2495872352

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475005_47475006delinsCT , CM000664.2:g.47475005_47475006delinsCT	GRCh38
NC_000002.11:g.47702144_47702145delinsCT , CM000664.1:g.47702144_47702145delinsCT	GRCh37
NC_000002.10:g.47555648_47555649delinsCT	NCBI36
NG_007110.2:g.76882_76883delinsCT , LRG_218:g.76882_76883delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1760-20_1760-19delinsCT	ENSP00000495641.2:n.1760-20_1760-19delinsCT
ENST00000233146.7:c.1760-20_1760-19delinsCT MANE Select	ENSP00000233146.2:n.1760-20_1760-19delinsCT
ENST00000543555.6:c.1562-20_1562-19delinsCT	ENSP00000442697.1:n.1562-20_1562-19delinsCT
ENST00000644092.1:c.*60-20_*60-19delinsCT	ENSP00000496351.1:n.*60-20_*60-19delinsCT
ENST00000645339.1:c.1760-20_1760-19delinsCT	ENSP00000496441.1:n.1760-20_1760-19delinsCT
ENST00000645506.1:c.1760-20_1760-19delinsCT	ENSP00000495455.1:n.1760-20_1760-19delinsCT
ENST00000646415.1:c.1760-20_1760-19delinsCT	ENSP00000495543.1:n.1760-20_1760-19delinsCT
ENST00000233146.6:c.1760-20_1760-19delinsCT	ENSP00000233146.2:n.1760-20_1760-19delinsCT
ENST00000406134.5:c.1760-20_1760-19delinsCT	ENSP00000384199.1:n.1760-20_1760-19delinsCT
ENST00000543555.5:c.1562-20_1562-19delinsCT	ENSP00000442697.1:n.1562-20_1562-19delinsCT
ENST00000610696.4:c.*156-20_*156-19delinsCT	ENSP00000483159.1:n.*156-20_*156-19delinsCT
ENST00000613514.4:c.*300-20_*300-19delinsCT	ENSP00000484137.1:n.*300-20_*300-19delinsCT
ENST00000617333.3:c.*526-20_*526-19delinsCT	ENSP00000482468.1:n.*526-20_*526-19delinsCT
ENST00000617938.4:c.*732-20_*732-19delinsCT	ENSP00000481158.1:n.*732-20_*732-19delinsCT
ENST00000621359.2:c.1760-20_1760-19delinsCT	ENSP00000481416.1:n.1760-20_1760-19delinsCT
NM_000251.2:c.1760-20_1760-19delinsCT , LRG_218t1:c.1760-20_1760-19delinsCT	NP_000242.1:n.1760-20_1760-19delinsCT
NM_001258281.1:c.1562-20_1562-19delinsCT	NP_001245210.1:n.1562-20_1562-19delinsCT
XM_005264332.2:c.1760-20_1760-19delinsCT	XP_005264389.2:n.1760-20_1760-19delinsCT
XM_011532867.1:c.1760-20_1760-19delinsCT	XP_011531169.1:n.1760-20_1760-19delinsCT
XR_939685.1:n.1832-20_1832-19delinsCT
XM_005264332.4:c.1760-20_1760-19delinsCT	XP_005264389.2:n.1760-20_1760-19delinsCT
XM_011532867.2:c.1760-20_1760-19delinsCT	XP_011531169.1:n.1760-20_1760-19delinsCT
XR_001738747.2:n.1822-20_1822-19delinsCT
XR_939685.2:n.1822-20_1822-19delinsCT
NM_000251.3:c.1760-20_1760-19delinsCT MANE Select	NP_000242.1:n.1760-20_1760-19delinsCT