Canonical Allele Identifier: CA022502
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91240
dbSNP Id: rs63750885

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47414374_47414375dup , CM000664.2:g.47414374_47414375dup GRCh38
NC_000002.11:g.47641513_47641514dup , CM000664.1:g.47641513_47641514dup GRCh37
NC_000002.10:g.47495017_47495018dup NCBI36
NG_007110.2:g.16251_16252dup , LRG_218:g.16251_16252dup

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.898_899dup ENSP00000495641.2:p.Met300IlefsTer2
ENST00000233146.7:c.898_899dup MANE Select ENSP00000233146.2:p.Met300IlefsTer2
ENST00000543555.6:c.700_701dup ENSP00000442697.1:p.Met234IlefsTer2
ENST00000644092.1:c.898_899dup ENSP00000496351.1:p.Met300IlefsTer2
ENST00000645339.1:c.898_899dup ENSP00000496441.1:p.Met300IlefsTer2
ENST00000645506.1:c.898_899dup ENSP00000495455.1:p.Met300IlefsTer2
ENST00000646415.1:c.898_899dup ENSP00000495543.1:p.Met300IlefsTer2
ENST00000233146.6:c.898_899dup ENSP00000233146.2:p.Met300IlefsTer2
ENST00000406134.5:c.898_899dup ENSP00000384199.1:p.Met300IlefsTer2
ENST00000543555.5:c.700_701dup ENSP00000442697.1:p.Met234IlefsTer2
ENST00000610696.4:c.898_899dup ENSP00000483159.1:p.Met300IlefsTer2
ENST00000613514.4:c.898_899dup ENSP00000484137.1:p.Met300IlefsTer2
ENST00000617333.3:c.898_899dup ENSP00000482468.1:p.Met300IlefsTer2
ENST00000617938.4:c.898_899dup ENSP00000481158.1:p.Met300IlefsTer2
ENST00000621359.2:c.898_899dup ENSP00000481416.1:p.Met300IlefsTer2
NM_000251.2:c.898_899dup , LRG_218t1:c.898_899dup NP_000242.1:p.Met300IlefsTer2
NM_001258281.1:c.700_701dup NP_001245210.1:p.Met234IlefsTer2
XM_005264332.2:c.898_899dup XP_005264389.2:p.Met300IlefsTer2
XM_011532867.1:c.898_899dup XP_011531169.1:p.Met300IlefsTer2
XR_939685.1:n.970_971dup
XM_005264332.4:c.898_899dup XP_005264389.2:p.Met300IlefsTer2
XM_011532867.2:c.898_899dup XP_011531169.1:p.Met300IlefsTer2
XR_001738747.2:n.960_961dup
XR_939685.2:n.960_961dup
NM_000251.3:c.898_899dup MANE Select NP_000242.1:p.Met300IlefsTer2