Canonical Allele Identifier: CA019953
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90877
ClinVar RCV Id: RCV000076379
dbSNP Id: rs63749878

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47476432dup , CM000664.2:g.47476432dup GRCh38
NC_000002.11:g.47703571dup , CM000664.1:g.47703571dup GRCh37
NC_000002.10:g.47557075dup NCBI36
NG_007110.2:g.78309dup , LRG_218:g.78309dup

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.2071dup ENSP00000495641.2:p.Ile691AsnfsTer8
ENST00000233146.7:c.2071dup MANE Select ENSP00000233146.2:p.Ile691AsnfsTer8
ENST00000543555.6:c.1873dup ENSP00000442697.1:p.Ile625AsnfsTer8
ENST00000644092.1:c.*371dup ENSP00000496351.1:n.*371dup
ENST00000645339.1:c.2071dup ENSP00000496441.1:p.Ile691AsnfsTer8
ENST00000645506.1:c.2071dup ENSP00000495455.1:p.Ile691AsnfsTer8
ENST00000646415.1:c.2071dup ENSP00000495543.1:p.Ile691AsnfsTer8
ENST00000233146.6:c.2071dup ENSP00000233146.2:p.Ile691AsnfsTer8
ENST00000406134.5:c.2071dup ENSP00000384199.1:p.Ile691AsnfsTer8
ENST00000543555.5:c.1873dup ENSP00000442697.1:p.Ile625AsnfsTer8
ENST00000610696.4:c.*467dup ENSP00000483159.1:n.*467dup
ENST00000613514.4:c.*611dup ENSP00000484137.1:n.*611dup
ENST00000617333.3:c.*837dup ENSP00000482468.1:n.*837dup
ENST00000617938.4:c.*1043dup ENSP00000481158.1:n.*1043dup
ENST00000621359.2:c.2071dup ENSP00000481416.1:p.Ile691AsnfsTer8
NM_000251.2:c.2071dup , LRG_218t1:c.2071dup NP_000242.1:p.Ile691AsnfsTer8
NM_001258281.1:c.1873dup NP_001245210.1:p.Ile625AsnfsTer8
XM_005264332.2:c.2071dup XP_005264389.2:p.Ile691AsnfsTer8
XM_011532867.1:c.2071dup XP_011531169.1:p.Ile691AsnfsTer8
XR_939685.1:n.2143dup
XM_005264332.4:c.2071dup XP_005264389.2:p.Ile691AsnfsTer8
XM_011532867.2:c.2071dup XP_011531169.1:p.Ile691AsnfsTer8
XR_001738747.2:n.2133dup
XR_939685.2:n.2133dup
NM_000251.3:c.2071dup MANE Select NP_000242.1:p.Ile691AsnfsTer8