Canonical Allele Identifier: CA2580066762
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1758350
ClinVar RCV Id: RCV002380146

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47429906_47429920del , CM000664.2:g.47429906_47429920del GRCh38
NC_000002.11:g.47657045_47657059del , CM000664.1:g.47657045_47657059del GRCh37
NC_000002.10:g.47510549_47510563del NCBI36
NG_007110.2:g.31783_31797del , LRG_218:g.31783_31797del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.1241_1255del ENSP00000495641.2:p.Leu414_Ile418del
ENST00000233146.7:c.1241_1255del MANE Select ENSP00000233146.2:p.Leu414_Ile418del
ENST00000543555.6:c.1043_1057del ENSP00000442697.1:p.Leu348_Ile352del
ENST00000644092.1:c.1241_1255del ENSP00000496351.1:p.Leu414_Ile418del
ENST00000645339.1:c.1241_1255del ENSP00000496441.1:p.Leu414_Ile418del
ENST00000645506.1:c.1241_1255del ENSP00000495455.1:p.Leu414_Ile418del
ENST00000646415.1:c.1241_1255del ENSP00000495543.1:p.Leu414_Ile418del
ENST00000233146.6:c.1241_1255del ENSP00000233146.2:p.Leu414_Ile418del
ENST00000406134.5:c.1241_1255del ENSP00000384199.1:p.Leu414_Ile418del
ENST00000543555.5:c.1043_1057del ENSP00000442697.1:p.Leu348_Ile352del
ENST00000610696.4:c.1241_1255del ENSP00000483159.1:p.Leu414_Ile418del
ENST00000613514.4:c.1241_1255del ENSP00000484137.1:p.Leu414_Ile418del
ENST00000617333.3:c.*7_*21del ENSP00000482468.1:n.*7_*21del
ENST00000617938.4:c.*213_*227del ENSP00000481158.1:n.*213_*227del
ENST00000621359.2:c.1241_1255del ENSP00000481416.1:p.Leu414_Ile418del
NM_000251.2:c.1241_1255del , LRG_218t1:c.1241_1255del NP_000242.1:p.Leu414_Ile418del
NM_001258281.1:c.1043_1057del NP_001245210.1:p.Leu348_Ile352del
XM_005264332.2:c.1241_1255del XP_005264389.2:p.Leu414_Ile418del
XM_011532867.1:c.1241_1255del XP_011531169.1:p.Leu414_Ile418del
XR_939685.1:n.1313_1327del
XM_005264332.4:c.1241_1255del XP_005264389.2:p.Leu414_Ile418del
XM_011532867.2:c.1241_1255del XP_011531169.1:p.Leu414_Ile418del
XR_001738747.2:n.1303_1317del
XR_939685.2:n.1303_1317del
NM_000251.3:c.1241_1255del MANE Select NP_000242.1:p.Leu414_Ile418del