Canonical Allele Identifier: CA2580067425
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796314
ClinVar RCV Id: RCV002441688

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47408469del , CM000664.2:g.47408469del GRCh38
NC_000002.11:g.47635608del , CM000664.1:g.47635608del GRCh37
NC_000002.10:g.47489112del NCBI36
NG_007110.2:g.10346del , LRG_218:g.10346del

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.280del ENSP00000495641.2:p.Leu94TrpfsTer?
ENST00000233146.7:c.280del MANE Select ENSP00000233146.2:p.Leu94TrpfsTer?
ENST00000543555.6:c.82del ENSP00000442697.1:p.Leu28TrpfsTer?
ENST00000644092.1:c.280del ENSP00000496351.1:p.Leu94TrpfsTer?
ENST00000645339.1:c.280del ENSP00000496441.1:p.Leu94TrpfsTer?
ENST00000645506.1:c.280del ENSP00000495455.1:p.Leu94TrpfsTer?
ENST00000646415.1:c.280del ENSP00000495543.1:p.Leu94TrpfsTer?
ENST00000233146.6:c.280del ENSP00000233146.2:p.Leu94TrpfsTer?
ENST00000406134.5:c.280del ENSP00000384199.1:p.Leu94TrpfsTer?
ENST00000454849.5:c.82del ENSP00000411482.1:p.Leu28TrpfsTer?
ENST00000543555.5:c.82del ENSP00000442697.1:p.Leu28TrpfsTer?
ENST00000610696.4:c.280del ENSP00000483159.1:p.Leu94TrpfsTer?
ENST00000613514.4:c.280del ENSP00000484137.1:p.Leu94TrpfsTer?
ENST00000617333.3:c.280del ENSP00000482468.1:p.Leu94TrpfsTer?
ENST00000617938.4:c.280del ENSP00000481158.1:p.Leu94TrpfsTer?
ENST00000621359.2:c.280del ENSP00000481416.1:p.Leu94TrpfsTer?
NM_000251.2:c.280del , LRG_218t1:c.280del NP_000242.1:p.Leu94TrpfsTer?
NM_001258281.1:c.82del NP_001245210.1:p.Leu28TrpfsTer?
XM_005264332.2:c.280del XP_005264389.2:p.Leu94TrpfsTer?
XM_011532867.1:c.280del XP_011531169.1:p.Leu94TrpfsTer?
XR_939685.1:n.352del
XM_005264332.4:c.280del XP_005264389.2:p.Leu94TrpfsTer?
XM_011532867.2:c.280del XP_011531169.1:p.Leu94TrpfsTer?
XR_001738747.2:n.342del
XR_939685.2:n.342del
NM_000251.3:c.280del MANE Select NP_000242.1:p.Leu94TrpfsTer?