Canonical Allele Identifier: CA1403107098

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756812C= , CM000665.2:g.133756812C=	GRCh38
NC_000003.11:g.133475656C= , CM000665.1:g.133475656C=	GRCh37
NC_000003.10:g.134958346C=	NCBI36
NG_013080.1:g.15680C=
NG_013080.2:g.99815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.692-19C= MANE Select	ENSP00000385834.3:n.692-19C=
ENST00000402696.7:c.692-19C=	ENSP00000385834.3:n.692-19C=
ENST00000482271.5:c.311-19C=	ENSP00000419338.1:n.311-19C=
ENST00000485977.1:c.158-120C=	ENSP00000418716.1:n.158-120C=
NM_001063.3:c.692-19C=	NP_001054.1:n.692-19C=
XM_011513100.1:c.692-19C=	XP_011511402.1:n.692-19C=
NM_001354703.1:c.560-19C=	NP_001341632.1:n.560-19C=
NM_001354704.1:c.311-19C=	NP_001341633.1:n.311-19C=
NM_001063.4:c.692-19C= MANE Select	NP_001054.2:n.692-19C=
NM_001354703.2:c.560-19C=	NP_001341632.2:n.560-19C=
NM_001354704.2:c.311-19C=	NP_001341633.2:n.311-19C=