Canonical Allele Identifier: CA2499216026

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1069135
• ClinVar RCV Id: RCV001380886
• dbSNP Id: rs2104174891

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414356_47414363dup , CM000664.2:g.47414356_47414363dup	GRCh38
NC_000002.11:g.47641495_47641502dup , CM000664.1:g.47641495_47641502dup	GRCh37
NC_000002.10:g.47494999_47495006dup	NCBI36
NG_007110.2:g.16233_16240dup , LRG_218:g.16233_16240dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.880_887dup	ENSP00000495641.2:p.Ser297LeufsTer7
ENST00000233146.7:c.880_887dup MANE Select	ENSP00000233146.2:p.Ser297LeufsTer7
ENST00000543555.6:c.682_689dup	ENSP00000442697.1:p.Ser231LeufsTer7
ENST00000644092.1:c.880_887dup	ENSP00000496351.1:p.Ser297LeufsTer7
ENST00000645339.1:c.880_887dup	ENSP00000496441.1:p.Ser297LeufsTer7
ENST00000645506.1:c.880_887dup	ENSP00000495455.1:p.Ser297LeufsTer7
ENST00000646415.1:c.880_887dup	ENSP00000495543.1:p.Ser297LeufsTer7
ENST00000233146.6:c.880_887dup	ENSP00000233146.2:p.Ser297LeufsTer7
ENST00000406134.5:c.880_887dup	ENSP00000384199.1:p.Ser297LeufsTer7
ENST00000543555.5:c.682_689dup	ENSP00000442697.1:p.Ser231LeufsTer7
ENST00000610696.4:c.880_887dup	ENSP00000483159.1:p.Ser297LeufsTer7
ENST00000613514.4:c.880_887dup	ENSP00000484137.1:p.Ser297LeufsTer7
ENST00000617333.3:c.880_887dup	ENSP00000482468.1:p.Ser297LeufsTer7
ENST00000617938.4:c.880_887dup	ENSP00000481158.1:p.Ser297LeufsTer7
ENST00000621359.2:c.880_887dup	ENSP00000481416.1:p.Ser297LeufsTer7
NM_000251.2:c.880_887dup , LRG_218t1:c.880_887dup	NP_000242.1:p.Ser297LeufsTer7
NM_001258281.1:c.682_689dup	NP_001245210.1:p.Ser231LeufsTer7
XM_005264332.2:c.880_887dup	XP_005264389.2:p.Ser297LeufsTer7
XM_011532867.1:c.880_887dup	XP_011531169.1:p.Ser297LeufsTer7
XR_939685.1:n.952_959dup
XM_005264332.4:c.880_887dup	XP_005264389.2:p.Ser297LeufsTer7
XM_011532867.2:c.880_887dup	XP_011531169.1:p.Ser297LeufsTer7
XR_001738747.2:n.942_949dup
XR_939685.2:n.942_949dup
NM_000251.3:c.880_887dup MANE Select	NP_000242.1:p.Ser297LeufsTer7