Canonical Allele Identifier: CA1403130604

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775291_133775292delinsTC , CM000665.2:g.133775291_133775292delinsTC	GRCh38
NC_000003.11:g.133494135_133494136delinsTC , CM000665.1:g.133494135_133494136delinsTC	GRCh37
NC_000003.10:g.134976825_134976826delinsTC	NCBI36
NG_013080.1:g.34159_34160delinsTC
NG_013080.2:g.118294_118295delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-142_1688-141delinsTC MANE Select	ENSP00000385834.3:n.1688-142_1688-141delinsTC
ENST00000402696.7:c.1688-142_1688-141delinsTC	ENSP00000385834.3:n.1688-142_1688-141delinsTC
ENST00000461695.1:c.419-142_419-141delinsTC
ENST00000467842.1:n.2540_2541delinsTC
NM_001063.3:c.1688-142_1688-141delinsTC	NP_001054.1:n.1688-142_1688-141delinsTC
XM_011513100.1:c.1688-142_1688-141delinsTC	XP_011511402.1:n.1688-142_1688-141delinsTC
NM_001354703.1:c.1556-142_1556-141delinsTC	NP_001341632.1:n.1556-142_1556-141delinsTC
NM_001354704.1:c.1307-142_1307-141delinsTC	NP_001341633.1:n.1307-142_1307-141delinsTC
NM_001063.4:c.1688-142_1688-141delinsTC MANE Select	NP_001054.2:n.1688-142_1688-141delinsTC
NM_001354703.2:c.1556-142_1556-141delinsTC	NP_001341632.2:n.1556-142_1556-141delinsTC
NM_001354704.2:c.1307-142_1307-141delinsTC	NP_001341633.2:n.1307-142_1307-141delinsTC