Canonical Allele Identifier: CA2580066989
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1761702
ClinVar RCV Id: RCV002419274

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47414278_47414289dup , CM000664.2:g.47414278_47414289dup GRCh38
NC_000002.11:g.47641417_47641428dup , CM000664.1:g.47641417_47641428dup GRCh37
NC_000002.10:g.47494921_47494932dup NCBI36
NG_007110.2:g.16155_16166dup , LRG_218:g.16155_16166dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.802_813dup ENSP00000495641.2:p.Ser271_Ala272insSerSerLeuSer
ENST00000233146.7:c.802_813dup MANE Select ENSP00000233146.2:p.Ser271_Ala272insSerSerLeuSer
ENST00000543555.6:c.604_615dup ENSP00000442697.1:p.Ser205_Ala206insSerSerLeuSer
ENST00000644092.1:c.802_813dup ENSP00000496351.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000645339.1:c.802_813dup ENSP00000496441.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000645506.1:c.802_813dup ENSP00000495455.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000646415.1:c.802_813dup ENSP00000495543.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000233146.6:c.802_813dup ENSP00000233146.2:p.Ser271_Ala272insSerSerLeuSer
ENST00000406134.5:c.802_813dup ENSP00000384199.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000543555.5:c.604_615dup ENSP00000442697.1:p.Ser205_Ala206insSerSerLeuSer
ENST00000610696.4:c.802_813dup ENSP00000483159.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000613514.4:c.802_813dup ENSP00000484137.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000617333.3:c.802_813dup ENSP00000482468.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000617938.4:c.802_813dup ENSP00000481158.1:p.Ser271_Ala272insSerSerLeuSer
ENST00000621359.2:c.802_813dup ENSP00000481416.1:p.Ser271_Ala272insSerSerLeuSer
NM_000251.2:c.802_813dup , LRG_218t1:c.802_813dup NP_000242.1:p.Ser271_Ala272insSerSerLeuSer
NM_001258281.1:c.604_615dup NP_001245210.1:p.Ser205_Ala206insSerSerLeuSer
XM_005264332.2:c.802_813dup XP_005264389.2:p.Ser271_Ala272insSerSerLeuSer
XM_011532867.1:c.802_813dup XP_011531169.1:p.Ser271_Ala272insSerSerLeuSer
XR_939685.1:n.874_885dup
XM_005264332.4:c.802_813dup XP_005264389.2:p.Ser271_Ala272insSerSerLeuSer
XM_011532867.2:c.802_813dup XP_011531169.1:p.Ser271_Ala272insSerSerLeuSer
XR_001738747.2:n.864_875dup
XR_939685.2:n.864_875dup
NM_000251.3:c.802_813dup MANE Select NP_000242.1:p.Ser271_Ala272insSerSerLeuSer