Canonical Allele Identifier: CA019751
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90847
dbSNP Id: rs267607991

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47476365A>G , CM000664.2:g.47476365A>G GRCh38
NC_000002.11:g.47703504A>G , CM000664.1:g.47703504A>G GRCh37
NC_000002.10:g.47557008A>G NCBI36
NG_007110.2:g.78242A>G , LRG_218:g.78242A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000233146.7:c.2006-2A>G MANE Select ENSP00000233146.2:p.=
ENST00000543555.6:c.1808-2A>G ENSP00000442697.1:p.=
ENST00000644092.1:c.*306-2A>G ENSP00000496351.1:p.=
ENST00000645339.1:c.2006-2A>G ENSP00000496441.1:p.=
ENST00000645506.1:c.2006-2A>G ENSP00000495455.1:p.=
ENST00000646415.1:c.2006-2A>G ENSP00000495543.1:p.=
ENST00000233146.6:c.2006-2A>G ENSP00000233146.2:p.=
ENST00000406134.5:c.2006-2A>G ENSP00000384199.1:p.=
ENST00000543555.5:c.1808-2A>G ENSP00000442697.1:p.=
ENST00000610696.4:c.*402-2A>G ENSP00000483159.1:p.=
ENST00000613514.4:c.*546-2A>G ENSP00000484137.1:p.=
ENST00000617333.3:c.*772-2A>G ENSP00000482468.1:p.=
ENST00000617938.4:c.*978-2A>G ENSP00000481158.1:p.=
ENST00000621359.2:c.2006-2A>G ENSP00000481416.1:p.=
NM_000251.2:c.2006-2A>G , LRG_218t1:c.2006-2A>G NP_000242.1:p.=
NM_001258281.1:c.1808-2A>G NP_001245210.1:p.=
XM_005264332.2:c.2006-2A>G XP_005264389.2:p.=
XM_011532867.1:c.2006-2A>G XP_011531169.1:p.=
XR_939685.1:n.2078-2A>G
XM_005264332.4:c.2006-2A>G XP_005264389.2:p.=
XM_011532867.2:c.2006-2A>G XP_011531169.1:p.=
XR_001738747.2:n.2068-2A>G
XR_939685.2:n.2068-2A>G
NM_000251.3:c.2006-2A>G MANE Select NP_000242.1:p.=