Canonical Allele Identifier: CA2699268416

Gene: MSH2

Linked Data

• dbSNP Id: rs2103975062

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47408400_47408454dup , CM000664.2:g.47408400_47408454dup	GRCh38
NC_000002.11:g.47635539_47635593dup , CM000664.1:g.47635539_47635593dup	GRCh37
NC_000002.10:g.47489043_47489097dup	NCBI36
NG_007110.2:g.10277_10331dup , LRG_218:g.10277_10331dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.212-1_265dup
ENST00000233146.7:c.212-1_265dup
ENST00000543555.6:c.14-1_67dup
ENST00000644092.1:c.212-1_265dup
ENST00000645339.1:c.212-1_265dup
ENST00000645506.1:c.212-1_265dup
ENST00000646415.1:c.212-1_265dup
ENST00000233146.6:c.212-1_265dup
ENST00000406134.5:c.212-1_265dup
ENST00000454849.5:c.14-1_67dup
ENST00000543555.5:c.14-1_67dup
ENST00000610696.4:c.212-1_265dup
ENST00000613514.4:c.212-1_265dup
ENST00000617333.3:c.212-1_265dup
ENST00000617938.4:c.212-1_265dup
ENST00000621359.2:c.212-1_265dup
NM_000251.2:c.212-1_265dup , LRG_218t1:c.212-1_265dup
NM_001258281.1:c.14-1_67dup
XM_005264332.2:c.212-1_265dup
XM_011532867.1:c.212-1_265dup
XR_939685.1:n.284-1_337dup
XM_005264332.4:c.212-1_265dup
XM_011532867.2:c.212-1_265dup
XR_001738747.2:n.274-1_327dup
XR_939685.2:n.274-1_327dup
NM_000251.3:c.212-1_265dup