Canonical Allele Identifier: CA2667757883
Gene: TOPBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133601066A>G , CM000665.2:g.133601066A>G GRCh38
NC_000003.11:g.133319910A>G , CM000665.1:g.133319910A>G GRCh37
NC_000003.10:g.134802600A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260810.10:c.*184T>C MANE Select ENSP00000260810.5:n.*184T>C
ENST00000642236.1:c.*184T>C ENSP00000493612.1:n.*184T>C
ENST00000260810.9:c.*184T>C ENSP00000260810.5:n.*184T>C
ENST00000503338.5:n.163-2436T>C
ENST00000503464.1:n.163-2436T>C
NM_007027.3:c.*184T>C NP_008958.2:n.*184T>C
XM_005247076.2:c.*184T>C XP_005247133.1:n.*184T>C
NM_001363889.1:c.*184T>C NP_001350818.1:n.*184T>C
XM_017005636.2:c.*184T>C XP_016861125.1:n.*184T>C
XM_017005637.2:c.*184T>C XP_016861126.1:n.*184T>C
XR_001739988.2:n.4781T>C
NM_001363889.2:c.*184T>C NP_001350818.1:n.*184T>C
NM_007027.4:c.*184T>C MANE Select NP_008958.2:n.*184T>C