Canonical Allele Identifier: CA2495873187
Gene: MSH2 HGNC NCBI

Linked Data

dbSNP Id: rs1667293079

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47476235_47476247del , CM000664.2:g.47476235_47476247del GRCh38
NC_000002.11:g.47703374_47703386del , CM000664.1:g.47703374_47703386del GRCh37
NC_000002.10:g.47556878_47556890del NCBI36
NG_007110.2:g.78112_78124del , LRG_218:g.78112_78124del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.2006-132_2006-120del ENSP00000495641.2:n.2006-132_2006-120del
ENST00000233146.7:c.2006-132_2006-120del MANE Select ENSP00000233146.2:n.2006-132_2006-120del
ENST00000543555.6:c.1808-132_1808-120del ENSP00000442697.1:n.1808-132_1808-120del
ENST00000644092.1:c.*306-132_*306-120del ENSP00000496351.1:n.*306-132_*306-120del
ENST00000645339.1:c.2006-132_2006-120del ENSP00000496441.1:n.2006-132_2006-120del
ENST00000645506.1:c.2006-132_2006-120del ENSP00000495455.1:n.2006-132_2006-120del
ENST00000646415.1:c.2006-132_2006-120del ENSP00000495543.1:n.2006-132_2006-120del
ENST00000233146.6:c.2006-132_2006-120del ENSP00000233146.2:n.2006-132_2006-120del
ENST00000406134.5:c.2006-132_2006-120del ENSP00000384199.1:n.2006-132_2006-120del
ENST00000543555.5:c.1808-132_1808-120del ENSP00000442697.1:n.1808-132_1808-120del
ENST00000610696.4:c.*402-132_*402-120del ENSP00000483159.1:n.*402-132_*402-120del
ENST00000613514.4:c.*546-132_*546-120del ENSP00000484137.1:n.*546-132_*546-120del
ENST00000617333.3:c.*772-132_*772-120del ENSP00000482468.1:n.*772-132_*772-120del
ENST00000617938.4:c.*978-132_*978-120del ENSP00000481158.1:n.*978-132_*978-120del
ENST00000621359.2:c.2006-132_2006-120del ENSP00000481416.1:n.2006-132_2006-120del
NM_000251.2:c.2006-132_2006-120del , LRG_218t1:c.2006-132_2006-120del NP_000242.1:n.2006-132_2006-120del
NM_001258281.1:c.1808-132_1808-120del NP_001245210.1:n.1808-132_1808-120del
XM_005264332.2:c.2006-132_2006-120del XP_005264389.2:n.2006-132_2006-120del
XM_011532867.1:c.2006-132_2006-120del XP_011531169.1:n.2006-132_2006-120del
XR_939685.1:n.2078-132_2078-120del
XM_005264332.4:c.2006-132_2006-120del XP_005264389.2:n.2006-132_2006-120del
XM_011532867.2:c.2006-132_2006-120del XP_011531169.1:n.2006-132_2006-120del
XR_001738747.2:n.2068-132_2068-120del
XR_939685.2:n.2068-132_2068-120del
NM_000251.3:c.2006-132_2006-120del MANE Select NP_000242.1:n.2006-132_2006-120del