Canonical Allele Identifier: CA1403050151
Gene: TOPBP1 HGNC NCBI

Linked Data

dbSNP Id: rs1934276822

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133601104A>T , CM000665.2:g.133601104A>T GRCh38
NC_000003.11:g.133319948A>T , CM000665.1:g.133319948A>T GRCh37
NC_000003.10:g.134802638A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260810.10:c.*146T>A MANE Select ENSP00000260810.5:n.*146T>A
ENST00000642236.1:c.*146T>A ENSP00000493612.1:n.*146T>A
ENST00000260810.9:c.*146T>A ENSP00000260810.5:n.*146T>A
ENST00000503338.5:n.163-2474T>A
ENST00000503464.1:n.163-2474T>A
NM_007027.3:c.*146T>A NP_008958.2:n.*146T>A
XM_005247076.2:c.*146T>A XP_005247133.1:n.*146T>A
NM_001363889.1:c.*146T>A NP_001350818.1:n.*146T>A
XM_017005636.2:c.*146T>A XP_016861125.1:n.*146T>A
XM_017005637.2:c.*146T>A XP_016861126.1:n.*146T>A
XR_001739988.2:n.4743T>A
NM_001363889.2:c.*146T>A NP_001350818.1:n.*146T>A
NM_007027.4:c.*146T>A MANE Select NP_008958.2:n.*146T>A