Canonical Allele Identifier: CA1403107182

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756872C= , CM000665.2:g.133756872C=	GRCh38
NC_000003.11:g.133475716C= , CM000665.1:g.133475716C=	GRCh37
NC_000003.10:g.134958406C=	NCBI36
NG_013080.1:g.15740C=
NG_013080.2:g.99875C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.733C= MANE Select	ENSP00000385834.3:p.Leu245=
ENST00000402696.7:c.733C=	ENSP00000385834.3:p.Leu245=
ENST00000482271.5:c.352C=	ENSP00000419338.1:p.Leu118=
ENST00000485977.1:c.158-60C=	ENSP00000418716.1:n.158-60C=
NM_001063.3:c.733C=	NP_001054.1:p.Leu245=
XM_011513100.1:c.733C=	XP_011511402.1:p.Leu245=
NM_001354703.1:c.601C=	NP_001341632.1:p.Leu201=
NM_001354704.1:c.352C=	NP_001341633.1:p.Leu118=
NM_001063.4:c.733C= MANE Select	NP_001054.2:p.Leu245=
NM_001354703.2:c.601C=	NP_001341632.2:p.Leu201=
NM_001354704.2:c.352C=	NP_001341633.2:p.Leu118=