Canonical Allele Identifier: CA1403050090

Gene: TOPBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133600970_133600974delinsAAAAT , CM000665.2:g.133600970_133600974delinsAAAAT	GRCh38
NC_000003.11:g.133319814_133319818delinsAAAAT , CM000665.1:g.133319814_133319818delinsAAAAT	GRCh37
NC_000003.10:g.134802504_134802508delinsAAAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260810.10:c.*276_*280delinsATTTT MANE Select	ENSP00000260810.5:n.*276_*280delinsATTTT
ENST00000642236.1:c.*276_*280delinsATTTT	ENSP00000493612.1:n.*276_*280delinsATTTT
ENST00000260810.9:c.*276_*280delinsATTTT	ENSP00000260810.5:n.*276_*280delinsATTTT
ENST00000503338.5:n.163-2344_163-2340delinsATTTT
ENST00000503464.1:n.163-2344_163-2340delinsATTTT
NM_007027.3:c.*276_*280delinsATTTT	NP_008958.2:n.*276_*280delinsATTTT
XM_005247076.2:c.*276_*280delinsATTTT	XP_005247133.1:n.*276_*280delinsATTTT
NM_001363889.1:c.*276_*280delinsATTTT	NP_001350818.1:n.*276_*280delinsATTTT
XM_017005636.2:c.*276_*280delinsATTTT	XP_016861125.1:n.*276_*280delinsATTTT
XM_017005637.2:c.*276_*280delinsATTTT	XP_016861126.1:n.*276_*280delinsATTTT
XR_001739988.2:n.4873_4877delinsATTTT
NM_001363889.2:c.*276_*280delinsATTTT	NP_001350818.1:n.*276_*280delinsATTTT
NM_007027.4:c.*276_*280delinsATTTT MANE Select	NP_008958.2:n.*276_*280delinsATTTT