Canonical Allele Identifier: CA1403107313

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756923T= , CM000665.2:g.133756923T=	GRCh38
NC_000003.11:g.133475767T= , CM000665.1:g.133475767T=	GRCh37
NC_000003.10:g.134958457T=	NCBI36
NG_013080.1:g.15791T=
NG_013080.2:g.99926T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.784T= MANE Select	ENSP00000385834.3:p.Leu262=
ENST00000402696.7:c.784T=	ENSP00000385834.3:p.Leu262=
ENST00000482271.5:c.403T=
ENST00000485977.1:c.158-9T=	ENSP00000418716.1:n.158-9T=
NM_001063.3:c.784T=	NP_001054.1:p.Leu262=
XM_011513100.1:c.784T=	XP_011511402.1:p.Leu262=
NM_001354703.1:c.652T=	NP_001341632.1:p.Leu218=
NM_001354704.1:c.403T=	NP_001341633.1:p.Leu135=
NM_001063.4:c.784T= MANE Select	NP_001054.2:p.Leu262=
NM_001354703.2:c.652T=	NP_001341632.2:p.Leu218=
NM_001354704.2:c.403T=	NP_001341633.2:p.Leu135=