Canonical Allele Identifier: CA2495832835

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412615_47412619delinsTAATA , CM000664.2:g.47412615_47412619delinsTAATA	GRCh38
NC_000002.11:g.47639754_47639758delinsTAATA , CM000664.1:g.47639754_47639758delinsTAATA	GRCh37
NC_000002.10:g.47493258_47493262delinsTAATA	NCBI36
NG_007110.2:g.14492_14496delinsTAATA , LRG_218:g.14492_14496delinsTAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.792+55_792+59delinsTAATA	ENSP00000495641.2:n.792+55_792+59delinsTAATA
ENST00000233146.7:c.792+55_792+59delinsTAATA MANE Select	ENSP00000233146.2:n.792+55_792+59delinsTAATA
ENST00000543555.6:c.594+55_594+59delinsTAATA	ENSP00000442697.1:n.594+55_594+59delinsTAATA
ENST00000644092.1:c.792+55_792+59delinsTAATA	ENSP00000496351.1:n.792+55_792+59delinsTAATA
ENST00000645339.1:c.792+55_792+59delinsTAATA	ENSP00000496441.1:n.792+55_792+59delinsTAATA
ENST00000645506.1:c.792+55_792+59delinsTAATA	ENSP00000495455.1:n.792+55_792+59delinsTAATA
ENST00000646415.1:c.792+55_792+59delinsTAATA	ENSP00000495543.1:n.792+55_792+59delinsTAATA
ENST00000233146.6:c.792+55_792+59delinsTAATA	ENSP00000233146.2:n.792+55_792+59delinsTAATA
ENST00000406134.5:c.792+55_792+59delinsTAATA	ENSP00000384199.1:n.792+55_792+59delinsTAATA
ENST00000543555.5:c.594+55_594+59delinsTAATA	ENSP00000442697.1:n.594+55_594+59delinsTAATA
ENST00000610696.4:c.792+55_792+59delinsTAATA	ENSP00000483159.1:n.792+55_792+59delinsTAATA
ENST00000613514.4:c.792+55_792+59delinsTAATA	ENSP00000484137.1:n.792+55_792+59delinsTAATA
ENST00000617333.3:c.792+55_792+59delinsTAATA	ENSP00000482468.1:n.792+55_792+59delinsTAATA
ENST00000617938.4:c.792+55_792+59delinsTAATA	ENSP00000481158.1:n.792+55_792+59delinsTAATA
ENST00000621359.2:c.792+55_792+59delinsTAATA	ENSP00000481416.1:n.792+55_792+59delinsTAATA
NM_000251.2:c.792+55_792+59delinsTAATA , LRG_218t1:c.792+55_792+59delinsTAATA	NP_000242.1:n.792+55_792+59delinsTAATA
NM_001258281.1:c.594+55_594+59delinsTAATA	NP_001245210.1:n.594+55_594+59delinsTAATA
XM_005264332.2:c.792+55_792+59delinsTAATA	XP_005264389.2:n.792+55_792+59delinsTAATA
XM_011532867.1:c.792+55_792+59delinsTAATA	XP_011531169.1:n.792+55_792+59delinsTAATA
XR_939685.1:n.864+55_864+59delinsTAATA
XM_005264332.4:c.792+55_792+59delinsTAATA	XP_005264389.2:n.792+55_792+59delinsTAATA
XM_011532867.2:c.792+55_792+59delinsTAATA	XP_011531169.1:n.792+55_792+59delinsTAATA
XR_001738747.2:n.854+55_854+59delinsTAATA
XR_939685.2:n.854+55_854+59delinsTAATA
NM_000251.3:c.792+55_792+59delinsTAATA MANE Select	NP_000242.1:n.792+55_792+59delinsTAATA