Canonical Allele Identifier: CA2695200751
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2673478
ClinVar RCV Id: RCV003450200

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403349_47403350dup , CM000664.2:g.47403349_47403350dup GRCh38
NC_000002.11:g.47630488_47630489dup , CM000664.1:g.47630488_47630489dup GRCh37
NC_000002.10:g.47483992_47483993dup NCBI36
NG_007110.2:g.5226_5227dup , LRG_218:g.5226_5227dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.158_159dup ENSP00000495641.2:p.Ala54ProfsTer11
ENST00000233146.7:c.158_159dup MANE Select ENSP00000233146.2:p.Ala54ProfsTer11
ENST00000543555.6:c.-30-11_-30-10dup ENSP00000442697.1:n.-30-11_-30-10dup
ENST00000644092.1:c.158_159dup ENSP00000496351.1:p.Ala54ProfsTer11
ENST00000645339.1:c.158_159dup ENSP00000496441.1:p.Ala54ProfsTer11
ENST00000645506.1:c.158_159dup ENSP00000495455.1:p.Ala54ProfsTer11
ENST00000646415.1:c.158_159dup ENSP00000495543.1:p.Ala54ProfsTer11
ENST00000233146.6:c.158_159dup ENSP00000233146.2:p.Ala54ProfsTer11
ENST00000406134.5:c.158_159dup ENSP00000384199.1:p.Ala54ProfsTer11
ENST00000454849.5:c.-30-11_-30-10dup ENSP00000411482.1:n.-30-11_-30-10dup
ENST00000543555.5:c.-30-11_-30-10dup ENSP00000442697.1:n.-30-11_-30-10dup
ENST00000610696.4:c.158_159dup ENSP00000483159.1:p.Ala54ProfsTer11
ENST00000613514.4:c.158_159dup ENSP00000484137.1:p.Ala54ProfsTer11
ENST00000617333.3:c.158_159dup ENSP00000482468.1:p.Ala54ProfsTer11
ENST00000617938.4:c.158_159dup ENSP00000481158.1:p.Ala54ProfsTer11
ENST00000621359.2:c.158_159dup ENSP00000481416.1:p.Ala54ProfsTer11
NM_000251.2:c.158_159dup , LRG_218t1:c.158_159dup NP_000242.1:p.Ala54ProfsTer11
NM_001258281.1:c.-30-11_-30-10dup NP_001245210.1:n.-30-11_-30-10dup
XM_005264332.2:c.158_159dup XP_005264389.2:p.Ala54ProfsTer11
XM_011532867.1:c.158_159dup XP_011531169.1:p.Ala54ProfsTer11
XR_939685.1:n.230_231dup
XM_005264332.4:c.158_159dup XP_005264389.2:p.Ala54ProfsTer11
XM_011532867.2:c.158_159dup XP_011531169.1:p.Ala54ProfsTer11
XR_001738747.2:n.220_221dup
XR_939685.2:n.220_221dup
NM_000251.3:c.158_159dup MANE Select NP_000242.1:p.Ala54ProfsTer11