Canonical Allele Identifier: CA2495872290

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47474920_47474921delinsTG , CM000664.2:g.47474920_47474921delinsTG	GRCh38
NC_000002.11:g.47702059_47702060delinsTG , CM000664.1:g.47702059_47702060delinsTG	GRCh37
NC_000002.10:g.47555563_47555564delinsTG	NCBI36
NG_007110.2:g.76797_76798delinsTG , LRG_218:g.76797_76798delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1760-105_1760-104delinsTG	ENSP00000495641.2:n.1760-105_1760-104delinsTG
ENST00000233146.7:c.1760-105_1760-104delinsTG MANE Select	ENSP00000233146.2:n.1760-105_1760-104delinsTG
ENST00000543555.6:c.1562-105_1562-104delinsTG	ENSP00000442697.1:n.1562-105_1562-104delinsTG
ENST00000644092.1:c.*60-105_*60-104delinsTG	ENSP00000496351.1:n.*60-105_*60-104delinsTG
ENST00000645339.1:c.1760-105_1760-104delinsTG	ENSP00000496441.1:n.1760-105_1760-104delinsTG
ENST00000645506.1:c.1760-105_1760-104delinsTG	ENSP00000495455.1:n.1760-105_1760-104delinsTG
ENST00000646415.1:c.1760-105_1760-104delinsTG	ENSP00000495543.1:n.1760-105_1760-104delinsTG
ENST00000233146.6:c.1760-105_1760-104delinsTG	ENSP00000233146.2:n.1760-105_1760-104delinsTG
ENST00000406134.5:c.1760-105_1760-104delinsTG	ENSP00000384199.1:n.1760-105_1760-104delinsTG
ENST00000543555.5:c.1562-105_1562-104delinsTG	ENSP00000442697.1:n.1562-105_1562-104delinsTG
ENST00000610696.4:c.*156-105_*156-104delinsTG	ENSP00000483159.1:n.*156-105_*156-104delinsTG
ENST00000613514.4:c.*300-105_*300-104delinsTG	ENSP00000484137.1:n.*300-105_*300-104delinsTG
ENST00000617333.3:c.*526-105_*526-104delinsTG	ENSP00000482468.1:n.*526-105_*526-104delinsTG
ENST00000617938.4:c.*732-105_*732-104delinsTG	ENSP00000481158.1:n.*732-105_*732-104delinsTG
ENST00000621359.2:c.1760-105_1760-104delinsTG	ENSP00000481416.1:n.1760-105_1760-104delinsTG
NM_000251.2:c.1760-105_1760-104delinsTG , LRG_218t1:c.1760-105_1760-104delinsTG	NP_000242.1:n.1760-105_1760-104delinsTG
NM_001258281.1:c.1562-105_1562-104delinsTG	NP_001245210.1:n.1562-105_1562-104delinsTG
XM_005264332.2:c.1760-105_1760-104delinsTG	XP_005264389.2:n.1760-105_1760-104delinsTG
XM_011532867.1:c.1760-105_1760-104delinsTG	XP_011531169.1:n.1760-105_1760-104delinsTG
XR_939685.1:n.1832-105_1832-104delinsTG
XM_005264332.4:c.1760-105_1760-104delinsTG	XP_005264389.2:n.1760-105_1760-104delinsTG
XM_011532867.2:c.1760-105_1760-104delinsTG	XP_011531169.1:n.1760-105_1760-104delinsTG
XR_001738747.2:n.1822-105_1822-104delinsTG
XR_939685.2:n.1822-105_1822-104delinsTG
NM_000251.3:c.1760-105_1760-104delinsTG MANE Select	NP_000242.1:n.1760-105_1760-104delinsTG