Canonical Allele Identifier: CA2667764573

Gene: TF

Linked Data

• gnomAD v4: 3-133757136-GTCACTAAGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757139_133757147del , CM000665.2:g.133757139_133757147del	GRCh38
NC_000003.11:g.133475983_133475991del , CM000665.1:g.133475983_133475991del	GRCh37
NC_000003.10:g.134958673_134958681del	NCBI36
NG_013080.1:g.16007_16015del
NG_013080.2:g.100142_100150del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+130_870+138del MANE Select	ENSP00000385834.3:n.870+130_870+138del
ENST00000402696.7:c.870+130_870+138del	ENSP00000385834.3:n.870+130_870+138del
ENST00000485977.1:c.235+130_235+138del	ENSP00000418716.1:n.235+130_235+138del
NM_001063.3:c.870+130_870+138del	NP_001054.1:n.870+130_870+138del
XM_011513100.1:c.870+130_870+138del	XP_011511402.1:n.870+130_870+138del
NM_001354703.1:c.738+130_738+138del	NP_001341632.1:n.738+130_738+138del
NM_001354704.1:c.489+130_489+138del	NP_001341633.1:n.489+130_489+138del
NM_001063.4:c.870+130_870+138del MANE Select	NP_001054.2:n.870+130_870+138del
NM_001354703.2:c.738+130_738+138del	NP_001341632.2:n.738+130_738+138del
NM_001354704.2:c.489+130_489+138del	NP_001341633.2:n.489+130_489+138del