Canonical Allele Identifier: CA425971026
Gene: MSH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.47709926A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47482787A>G , CM000664.2:g.47482787A>G GRCh38
NC_000002.11:g.47709926A>G , CM000664.1:g.47709926A>G GRCh37
NC_000002.10:g.47563430A>G NCBI36
NG_007110.2:g.84664A>G , LRG_218:g.84664A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.2634+1916A>G ENSP00000495641.2:n.2634+1916A>G
ENST00000233146.7:c.2643A>G MANE Select ENSP00000233146.2:p.Glu881=
ENST00000543555.6:c.2445A>G ENSP00000442697.1:p.Glu815=
ENST00000644092.1:c.*934+1916A>G ENSP00000496351.1:n.*934+1916A>G
ENST00000644900.1:c.487+1916A>G
ENST00000645339.1:c.2634+1916A>G ENSP00000496441.1:n.2634+1916A>G
ENST00000645506.1:c.2634+1916A>G ENSP00000495455.1:n.2634+1916A>G
ENST00000646415.1:c.2634+1916A>G ENSP00000495543.1:n.2634+1916A>G
ENST00000233146.6:c.2643A>G ENSP00000233146.2:p.Glu881=
ENST00000406134.5:c.2634+1916A>G ENSP00000384199.1:n.2634+1916A>G
ENST00000461394.5:n.75+1916A>G
ENST00000543555.5:c.2445A>G ENSP00000442697.1:p.Glu815=
ENST00000610696.4:c.*1039A>G ENSP00000483159.1:n.*1039A>G
ENST00000613514.4:c.*1183A>G ENSP00000484137.1:n.*1183A>G
ENST00000617333.3:c.*1409A>G ENSP00000482468.1:n.*1409A>G
ENST00000617938.4:c.*1615A>G ENSP00000481158.1:n.*1615A>G
ENST00000621359.2:c.*209A>G ENSP00000481416.1:n.*209A>G
NM_000251.2:c.2643A>G , LRG_218t1:c.2643A>G NP_000242.1:p.Glu881=
NM_001258281.1:c.2445A>G NP_001245210.1:p.Glu815=
XM_005264332.2:c.2634+1916A>G XP_005264389.2:n.2634+1916A>G
XM_011532867.1:c.2634+1916A>G XP_011531169.1:n.2634+1916A>G
XR_939685.1:n.2706+1916A>G
XM_005264332.4:c.2634+1916A>G XP_005264389.2:n.2634+1916A>G
XM_011532867.2:c.2634+1916A>G XP_011531169.1:n.2634+1916A>G
XR_001738747.2:n.2696+1916A>G
XR_939685.2:n.2696+1916A>G
NM_000251.3:c.2643A>G MANE Select NP_000242.1:p.Glu881=