Canonical Allele Identifier: CA346731306
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428556
ClinVar RCV Id: RCV000491804

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47482778G>A , CM000664.2:g.47482778G>A GRCh38
NC_000002.11:g.47709917G>A , CM000664.1:g.47709917G>A GRCh37
NC_000002.10:g.47563421G>A NCBI36
NG_007110.2:g.84655G>A , LRG_218:g.84655G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233146.7:c.2635-1G>A MANE Select ENSP00000233146.2:p.=
ENST00000543555.6:c.2437-1G>A ENSP00000442697.1:p.=
ENST00000644092.1:c.*934+1907G>A ENSP00000496351.1:p.=
ENST00000644900.1:n.487+1907G>A
ENST00000645339.1:c.2634+1907G>A ENSP00000496441.1:p.=
ENST00000645506.1:c.2634+1907G>A ENSP00000495455.1:p.=
ENST00000646415.1:c.2634+1907G>A ENSP00000495543.1:p.=
ENST00000233146.6:c.2635-1G>A ENSP00000233146.2:p.=
ENST00000406134.5:c.2634+1907G>A ENSP00000384199.1:p.=
ENST00000461394.5:n.75+1907G>A
ENST00000543555.5:c.2437-1G>A ENSP00000442697.1:p.=
ENST00000610696.4:c.*1031-1G>A ENSP00000483159.1:p.=
ENST00000613514.4:c.*1175-1G>A ENSP00000484137.1:p.=
ENST00000617333.3:c.*1401-1G>A ENSP00000482468.1:p.=
ENST00000617938.4:c.*1607-1G>A ENSP00000481158.1:p.=
ENST00000621359.2:c.*201-1G>A ENSP00000481416.1:p.=
NM_000251.2:c.2635-1G>A , LRG_218t1:c.2635-1G>A NP_000242.1:p.=
NM_001258281.1:c.2437-1G>A NP_001245210.1:p.=
XM_005264332.2:c.2634+1907G>A XP_005264389.2:p.=
XM_011532867.1:c.2634+1907G>A XP_011531169.1:p.=
XR_939685.1:n.2706+1907G>A
XM_005264332.4:c.2634+1907G>A XP_005264389.2:p.=
XM_011532867.2:c.2634+1907G>A XP_011531169.1:p.=
XR_001738747.2:n.2696+1907G>A
XR_939685.2:n.2696+1907G>A
NM_000251.3:c.2635-1G>A MANE Select NP_000242.1:p.=