Canonical Allele Identifier: CA2658948407
Gene: MSH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47476281_47476300del , CM000664.2:g.47476281_47476300del GRCh38
NC_000002.11:g.47703420_47703439del , CM000664.1:g.47703420_47703439del GRCh37
NC_000002.10:g.47556924_47556943del NCBI36
NG_007110.2:g.78158_78177del , LRG_218:g.78158_78177del

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.2006-86_2006-67del ENSP00000495641.2:n.2006-86_2006-67del
ENST00000233146.7:c.2006-86_2006-67del MANE Select ENSP00000233146.2:n.2006-86_2006-67del
ENST00000543555.6:c.1808-86_1808-67del ENSP00000442697.1:n.1808-86_1808-67del
ENST00000644092.1:c.*306-86_*306-67del ENSP00000496351.1:n.*306-86_*306-67del
ENST00000645339.1:c.2006-86_2006-67del ENSP00000496441.1:n.2006-86_2006-67del
ENST00000645506.1:c.2006-86_2006-67del ENSP00000495455.1:n.2006-86_2006-67del
ENST00000646415.1:c.2006-86_2006-67del ENSP00000495543.1:n.2006-86_2006-67del
ENST00000233146.6:c.2006-86_2006-67del ENSP00000233146.2:n.2006-86_2006-67del
ENST00000406134.5:c.2006-86_2006-67del ENSP00000384199.1:n.2006-86_2006-67del
ENST00000543555.5:c.1808-86_1808-67del ENSP00000442697.1:n.1808-86_1808-67del
ENST00000610696.4:c.*402-86_*402-67del ENSP00000483159.1:n.*402-86_*402-67del
ENST00000613514.4:c.*546-86_*546-67del ENSP00000484137.1:n.*546-86_*546-67del
ENST00000617333.3:c.*772-86_*772-67del ENSP00000482468.1:n.*772-86_*772-67del
ENST00000617938.4:c.*978-86_*978-67del ENSP00000481158.1:n.*978-86_*978-67del
ENST00000621359.2:c.2006-86_2006-67del ENSP00000481416.1:n.2006-86_2006-67del
NM_000251.2:c.2006-86_2006-67del , LRG_218t1:c.2006-86_2006-67del NP_000242.1:n.2006-86_2006-67del
NM_001258281.1:c.1808-86_1808-67del NP_001245210.1:n.1808-86_1808-67del
XM_005264332.2:c.2006-86_2006-67del XP_005264389.2:n.2006-86_2006-67del
XM_011532867.1:c.2006-86_2006-67del XP_011531169.1:n.2006-86_2006-67del
XR_939685.1:n.2078-86_2078-67del
XM_005264332.4:c.2006-86_2006-67del XP_005264389.2:n.2006-86_2006-67del
XM_011532867.2:c.2006-86_2006-67del XP_011531169.1:n.2006-86_2006-67del
XR_001738747.2:n.2068-86_2068-67del
XR_939685.2:n.2068-86_2068-67del
NM_000251.3:c.2006-86_2006-67del MANE Select NP_000242.1:n.2006-86_2006-67del