Canonical Allele Identifier: CA1403050126

Gene: TOPBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133601038T= , CM000665.2:g.133601038T=	GRCh38
NC_000003.11:g.133319882T= , CM000665.1:g.133319882T=	GRCh37
NC_000003.10:g.134802572T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260810.10:c.*212A= MANE Select	ENSP00000260810.5:n.*212A=
ENST00000642236.1:c.*212A=	ENSP00000493612.1:n.*212A=
ENST00000260810.9:c.*212A=	ENSP00000260810.5:n.*212A=
ENST00000503338.5:n.163-2408A=
ENST00000503464.1:n.163-2408A=
NM_007027.3:c.*212A=	NP_008958.2:n.*212A=
XM_005247076.2:c.*212A=	XP_005247133.1:n.*212A=
NM_001363889.1:c.*212A=	NP_001350818.1:n.*212A=
XM_017005636.2:c.*212A=	XP_016861125.1:n.*212A=
XM_017005637.2:c.*212A=	XP_016861126.1:n.*212A=
XR_001739988.2:n.4809A=
NM_001363889.2:c.*212A=	NP_001350818.1:n.*212A=
NM_007027.4:c.*212A= MANE Select	NP_008958.2:n.*212A=