Canonical Allele Identifier: CA1403049967

Gene: TOPBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133600737C= , CM000665.2:g.133600737C=	GRCh38
NC_000003.11:g.133319581C= , CM000665.1:g.133319581C=	GRCh37
NC_000003.10:g.134802271C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260810.10:c.*513G= MANE Select	ENSP00000260810.5:n.*513G=
ENST00000642236.1:c.*513G=	ENSP00000493612.1:n.*513G=
ENST00000260810.9:c.*513G=	ENSP00000260810.5:n.*513G=
ENST00000503338.5:n.163-2107G=
ENST00000503464.1:n.163-2107G=
NM_007027.3:c.*513G=	NP_008958.2:n.*513G=
XM_005247076.2:c.*513G=	XP_005247133.1:n.*513G=
NM_001363889.1:c.*513G=	NP_001350818.1:n.*513G=
XM_017005636.2:c.*513G=	XP_016861125.1:n.*513G=
XM_017005637.2:c.*513G=	XP_016861126.1:n.*513G=
XR_001739988.2:n.5110G=
NM_001363889.2:c.*513G=	NP_001350818.1:n.*513G=
NM_007027.4:c.*513G= MANE Select	NP_008958.2:n.*513G=