Canonical Allele Identifier: CA1403107450

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756986T= , CM000665.2:g.133756986T=	GRCh38
NC_000003.11:g.133475830T= , CM000665.1:g.133475830T=	GRCh37
NC_000003.10:g.134958520T=	NCBI36
NG_013080.1:g.15854T=
NG_013080.2:g.99989T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.847T= MANE Select	ENSP00000385834.3:p.Trp283=
ENST00000402696.7:c.847T=	ENSP00000385834.3:p.Trp283=
ENST00000485977.1:c.212T=	ENSP00000418716.1:p.Leu71=
NM_001063.3:c.847T=	NP_001054.1:p.Trp283=
XM_011513100.1:c.847T=	XP_011511402.1:p.Trp283=
NM_001354703.1:c.715T=	NP_001341632.1:p.Trp239=
NM_001354704.1:c.466T=	NP_001341633.1:p.Trp156=
NM_001063.4:c.847T= MANE Select	NP_001054.2:p.Trp283=
NM_001354703.2:c.715T=	NP_001341632.2:p.Trp239=
NM_001354704.2:c.466T=	NP_001341633.2:p.Trp156=