Canonical Allele Identifier: CA1403119284

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766255_133766256delinsCT , CM000665.2:g.133766255_133766256delinsCT	GRCh38
NC_000003.11:g.133485099_133485100delinsCT , CM000665.1:g.133485099_133485100delinsCT	GRCh37
NC_000003.10:g.134967789_134967790delinsCT	NCBI36
NG_013080.1:g.25123_25124delinsCT
NG_013080.2:g.109258_109259delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1331-23_1331-22delinsCT MANE Select	ENSP00000385834.3:n.1331-23_1331-22delinsCT
ENST00000402696.7:c.1331-23_1331-22delinsCT	ENSP00000385834.3:n.1331-23_1331-22delinsCT
NM_001063.3:c.1331-23_1331-22delinsCT	NP_001054.1:n.1331-23_1331-22delinsCT
XM_011513100.1:c.1331-23_1331-22delinsCT	XP_011511402.1:n.1331-23_1331-22delinsCT
NM_001354703.1:c.1199-23_1199-22delinsCT	NP_001341632.1:n.1199-23_1199-22delinsCT
NM_001354704.1:c.950-23_950-22delinsCT	NP_001341633.1:n.950-23_950-22delinsCT
NM_001063.4:c.1331-23_1331-22delinsCT MANE Select	NP_001054.2:n.1331-23_1331-22delinsCT
NM_001354703.2:c.1199-23_1199-22delinsCT	NP_001341632.2:n.1199-23_1199-22delinsCT
NM_001354704.2:c.950-23_950-22delinsCT	NP_001341633.2:n.950-23_950-22delinsCT