Canonical Allele Identifier: CA1139656934
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 973427
ClinVar RCV Id: RCV001250027
dbSNP Id: rs267607920

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47408452_47408453dup , CM000664.2:g.47408452_47408453dup GRCh38
NC_000002.11:g.47635591_47635592dup , CM000664.1:g.47635591_47635592dup GRCh37
NC_000002.10:g.47489095_47489096dup NCBI36
NG_007110.2:g.10329_10330dup , LRG_218:g.10329_10330dup

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.263_264dup ENSP00000495641.2:p.Val89LeufsTer2
ENST00000233146.7:c.263_264dup MANE Select ENSP00000233146.2:p.Val89LeufsTer2
ENST00000543555.6:c.65_66dup ENSP00000442697.1:p.Val23LeufsTer2
ENST00000644092.1:c.263_264dup ENSP00000496351.1:p.Val89LeufsTer2
ENST00000645339.1:c.263_264dup ENSP00000496441.1:p.Val89LeufsTer2
ENST00000645506.1:c.263_264dup ENSP00000495455.1:p.Val89LeufsTer2
ENST00000646415.1:c.263_264dup ENSP00000495543.1:p.Val89LeufsTer2
ENST00000233146.6:c.263_264dup ENSP00000233146.2:p.Val89LeufsTer2
ENST00000406134.5:c.263_264dup ENSP00000384199.1:p.Val89LeufsTer2
ENST00000454849.5:c.65_66dup ENSP00000411482.1:p.Val23LeufsTer2
ENST00000543555.5:c.65_66dup ENSP00000442697.1:p.Val23LeufsTer2
ENST00000610696.4:c.263_264dup ENSP00000483159.1:p.Val89LeufsTer2
ENST00000613514.4:c.263_264dup ENSP00000484137.1:p.Val89LeufsTer2
ENST00000617333.3:c.263_264dup ENSP00000482468.1:p.Val89LeufsTer2
ENST00000617938.4:c.263_264dup ENSP00000481158.1:p.Val89LeufsTer2
ENST00000621359.2:c.263_264dup ENSP00000481416.1:p.Val89LeufsTer2
NM_000251.2:c.263_264dup , LRG_218t1:c.263_264dup NP_000242.1:p.Val89LeufsTer2
NM_001258281.1:c.65_66dup NP_001245210.1:p.Val23LeufsTer2
XM_005264332.2:c.263_264dup XP_005264389.2:p.Val89LeufsTer2
XM_011532867.1:c.263_264dup XP_011531169.1:p.Val89LeufsTer2
XR_939685.1:n.335_336dup
XM_005264332.4:c.263_264dup XP_005264389.2:p.Val89LeufsTer2
XM_011532867.2:c.263_264dup XP_011531169.1:p.Val89LeufsTer2
XR_001738747.2:n.325_326dup
XR_939685.2:n.325_326dup
NM_000251.3:c.263_264dup MANE Select NP_000242.1:p.Val89LeufsTer2