Canonical Allele Identifier: CA2495865269

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47463105_47463107delinsCTT , CM000664.2:g.47463105_47463107delinsCTT	GRCh38
NC_000002.11:g.47690244_47690246delinsCTT , CM000664.1:g.47690244_47690246delinsCTT	GRCh37
NC_000002.10:g.47543748_47543750delinsCTT	NCBI36
NG_007110.2:g.64982_64984delinsCTT , LRG_218:g.64982_64984delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1461_1463delinsCTT	ENSP00000495641.2:p.Asp487=
ENST00000233146.7:c.1461_1463delinsCTT MANE Select	ENSP00000233146.2:p.Asp487=
ENST00000543555.6:c.1263_1265delinsCTT	ENSP00000442697.1:p.Asp421=
ENST00000644092.1:c.1461_1463delinsCTT	ENSP00000496351.1:p.Asp487=
ENST00000645339.1:c.1461_1463delinsCTT	ENSP00000496441.1:p.Asp487=
ENST00000645506.1:c.1461_1463delinsCTT	ENSP00000495455.1:p.Asp487=
ENST00000646415.1:c.1461_1463delinsCTT	ENSP00000495543.1:p.Asp487=
ENST00000233146.6:c.1461_1463delinsCTT	ENSP00000233146.2:p.Asp487=
ENST00000406134.5:c.1461_1463delinsCTT	ENSP00000384199.1:p.Asp487=
ENST00000543555.5:c.1263_1265delinsCTT	ENSP00000442697.1:p.Asp421=
ENST00000610696.4:c.1461_1463delinsCTT	ENSP00000483159.1:p.Asp487=
ENST00000613514.4:c.*1_*3delinsCTT	ENSP00000484137.1:n.*1_*3delinsCTT
ENST00000617333.3:c.*227_*229delinsCTT	ENSP00000482468.1:n.*227_*229delinsCTT
ENST00000617938.4:c.*433_*435delinsCTT	ENSP00000481158.1:n.*433_*435delinsCTT
ENST00000621359.2:c.1461_1463delinsCTT	ENSP00000481416.1:p.Asp487=
NM_000251.2:c.1461_1463delinsCTT , LRG_218t1:c.1461_1463delinsCTT	NP_000242.1:p.Asp487=
NM_001258281.1:c.1263_1265delinsCTT	NP_001245210.1:p.Asp421=
XM_005264332.2:c.1461_1463delinsCTT	XP_005264389.2:p.Asp487=
XM_011532867.1:c.1461_1463delinsCTT	XP_011531169.1:p.Asp487=
XR_939685.1:n.1533_1535delinsCTT
XM_005264332.4:c.1461_1463delinsCTT	XP_005264389.2:p.Asp487=
XM_011532867.2:c.1461_1463delinsCTT	XP_011531169.1:p.Asp487=
XR_001738747.2:n.1523_1525delinsCTT
XR_939685.2:n.1523_1525delinsCTT
NM_000251.3:c.1461_1463delinsCTT MANE Select	NP_000242.1:p.Asp487=