Canonical Allele Identifier: CA1403050129

Gene: TOPBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133601047A= , CM000665.2:g.133601047A=	GRCh38
NC_000003.11:g.133319891A= , CM000665.1:g.133319891A=	GRCh37
NC_000003.10:g.134802581A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260810.10:c.*203T= MANE Select	ENSP00000260810.5:n.*203T=
ENST00000642236.1:c.*203T=	ENSP00000493612.1:n.*203T=
ENST00000260810.9:c.*203T=	ENSP00000260810.5:n.*203T=
ENST00000503338.5:n.163-2417T=
ENST00000503464.1:n.163-2417T=
NM_007027.3:c.*203T=	NP_008958.2:n.*203T=
XM_005247076.2:c.*203T=	XP_005247133.1:n.*203T=
NM_001363889.1:c.*203T=	NP_001350818.1:n.*203T=
XM_017005636.2:c.*203T=	XP_016861125.1:n.*203T=
XM_017005637.2:c.*203T=	XP_016861126.1:n.*203T=
XR_001739988.2:n.4800T=
NM_001363889.2:c.*203T=	NP_001350818.1:n.*203T=
NM_007027.4:c.*203T= MANE Select	NP_008958.2:n.*203T=