Canonical Allele Identifier: CA1403107574

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757095_133757096delinsGA , CM000665.2:g.133757095_133757096delinsGA	GRCh38
NC_000003.11:g.133475939_133475940delinsGA , CM000665.1:g.133475939_133475940delinsGA	GRCh37
NC_000003.10:g.134958629_134958630delinsGA	NCBI36
NG_013080.1:g.15963_15964delinsGA
NG_013080.2:g.100098_100099delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+86_870+87delinsGA MANE Select	ENSP00000385834.3:n.870+86_870+87delinsGA
ENST00000402696.7:c.870+86_870+87delinsGA	ENSP00000385834.3:n.870+86_870+87delinsGA
ENST00000485977.1:c.235+86_235+87delinsGA	ENSP00000418716.1:n.235+86_235+87delinsGA
NM_001063.3:c.870+86_870+87delinsGA	NP_001054.1:n.870+86_870+87delinsGA
XM_011513100.1:c.870+86_870+87delinsGA	XP_011511402.1:n.870+86_870+87delinsGA
NM_001354703.1:c.738+86_738+87delinsGA	NP_001341632.1:n.738+86_738+87delinsGA
NM_001354704.1:c.489+86_489+87delinsGA	NP_001341633.1:n.489+86_489+87delinsGA
NM_001063.4:c.870+86_870+87delinsGA MANE Select	NP_001054.2:n.870+86_870+87delinsGA
NM_001354703.2:c.738+86_738+87delinsGA	NP_001341632.2:n.738+86_738+87delinsGA
NM_001354704.2:c.489+86_489+87delinsGA	NP_001341633.2:n.489+86_489+87delinsGA