Canonical Allele Identifier: CA019097
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90759
ClinVar RCV Id: RCV000076256
dbSNP Id: rs267607974

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47471020del , CM000664.2:g.47471020del GRCh38
NC_000002.11:g.47698159del , CM000664.1:g.47698159del GRCh37
NC_000002.10:g.47551663del NCBI36
NG_007110.2:g.72897del , LRG_218:g.72897del

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.1717del ENSP00000495641.2:p.Ala573ProfsTer17
ENST00000233146.7:c.1717del MANE Select ENSP00000233146.2:p.Ala573ProfsTer17
ENST00000543555.6:c.1519del ENSP00000442697.1:p.Ala507ProfsTer17
ENST00000644092.1:c.*17del ENSP00000496351.1:n.*17del
ENST00000645339.1:c.1717del ENSP00000496441.1:p.Ala573ProfsTer17
ENST00000645506.1:c.1717del ENSP00000495455.1:p.Ala573ProfsTer17
ENST00000646415.1:c.1717del ENSP00000495543.1:p.Ala573ProfsTer17
ENST00000233146.6:c.1717del ENSP00000233146.2:p.Ala573ProfsTer17
ENST00000406134.5:c.1717del ENSP00000384199.1:p.Ala573ProfsTer17
ENST00000543555.5:c.1519del ENSP00000442697.1:p.Ala507ProfsTer17
ENST00000610696.4:c.*113del ENSP00000483159.1:n.*113del
ENST00000613514.4:c.*257del ENSP00000484137.1:n.*257del
ENST00000617333.3:c.*483del ENSP00000482468.1:n.*483del
ENST00000617938.4:c.*689del ENSP00000481158.1:n.*689del
ENST00000621359.2:c.1717del ENSP00000481416.1:p.Ala573ProfsTer17
NM_000251.2:c.1717del , LRG_218t1:c.1717del NP_000242.1:p.Ala573ProfsTer17
NM_001258281.1:c.1519del NP_001245210.1:p.Ala507ProfsTer17
XM_005264332.2:c.1717del XP_005264389.2:p.Ala573ProfsTer17
XM_011532867.1:c.1717del XP_011531169.1:p.Ala573ProfsTer17
XR_939685.1:n.1789del
XM_005264332.4:c.1717del XP_005264389.2:p.Ala573ProfsTer17
XM_011532867.2:c.1717del XP_011531169.1:p.Ala573ProfsTer17
XR_001738747.2:n.1779del
XR_939685.2:n.1779del
NM_000251.3:c.1717del MANE Select NP_000242.1:p.Ala573ProfsTer17