Canonical Allele Identifier: CA2699275827
Gene: MSH2 HGNC NCBI

Linked Data

dbSNP Id: rs2104170023

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47414317_47414319del , CM000664.2:g.47414317_47414319del GRCh38
NC_000002.11:g.47641456_47641458del , CM000664.1:g.47641456_47641458del GRCh37
NC_000002.10:g.47494960_47494962del NCBI36
NG_007110.2:g.16194_16196del , LRG_218:g.16194_16196del

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.841_843del ENSP00000495641.2:p.Ser281del
ENST00000233146.7:c.841_843del MANE Select ENSP00000233146.2:p.Ser281del
ENST00000543555.6:c.643_645del ENSP00000442697.1:p.Ser215del
ENST00000644092.1:c.841_843del ENSP00000496351.1:p.Ser281del
ENST00000645339.1:c.841_843del ENSP00000496441.1:p.Ser281del
ENST00000645506.1:c.841_843del ENSP00000495455.1:p.Ser281del
ENST00000646415.1:c.841_843del ENSP00000495543.1:p.Ser281del
ENST00000233146.6:c.841_843del ENSP00000233146.2:p.Ser281del
ENST00000406134.5:c.841_843del ENSP00000384199.1:p.Ser281del
ENST00000543555.5:c.643_645del ENSP00000442697.1:p.Ser215del
ENST00000610696.4:c.841_843del ENSP00000483159.1:p.Ser281del
ENST00000613514.4:c.841_843del ENSP00000484137.1:p.Ser281del
ENST00000617333.3:c.841_843del ENSP00000482468.1:p.Ser281del
ENST00000617938.4:c.841_843del ENSP00000481158.1:p.Ser281del
ENST00000621359.2:c.841_843del ENSP00000481416.1:p.Ser281del
NM_000251.2:c.841_843del , LRG_218t1:c.841_843del NP_000242.1:p.Ser281del
NM_001258281.1:c.643_645del NP_001245210.1:p.Ser215del
XM_005264332.2:c.841_843del XP_005264389.2:p.Ser281del
XM_011532867.1:c.841_843del XP_011531169.1:p.Ser281del
XR_939685.1:n.913_915del
XM_005264332.4:c.841_843del XP_005264389.2:p.Ser281del
XM_011532867.2:c.841_843del XP_011531169.1:p.Ser281del
XR_001738747.2:n.903_905del
XR_939685.2:n.903_905del
NM_000251.3:c.841_843del MANE Select NP_000242.1:p.Ser281del