Canonical Allele Identifier: CA1403107129

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756837T= , CM000665.2:g.133756837T=	GRCh38
NC_000003.11:g.133475681T= , CM000665.1:g.133475681T=	GRCh37
NC_000003.10:g.134958371T=	NCBI36
NG_013080.1:g.15705T=
NG_013080.2:g.99840T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.698T= MANE Select	ENSP00000385834.3:p.Leu233=
ENST00000402696.7:c.698T=	ENSP00000385834.3:p.Leu233=
ENST00000482271.5:c.317T=	ENSP00000419338.1:p.Leu106=
ENST00000485977.1:c.158-95T=	ENSP00000418716.1:n.158-95T=
NM_001063.3:c.698T=	NP_001054.1:p.Leu233=
XM_011513100.1:c.698T=	XP_011511402.1:p.Leu233=
NM_001354703.1:c.566T=	NP_001341632.1:p.Leu189=
NM_001354704.1:c.317T=	NP_001341633.1:p.Leu106=
NM_001063.4:c.698T= MANE Select	NP_001054.2:p.Leu233=
NM_001354703.2:c.566T=	NP_001341632.2:p.Leu189=
NM_001354704.2:c.317T=	NP_001341633.2:p.Leu106=