Canonical Allele Identifier: CA1403107261

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756896C= , CM000665.2:g.133756896C=	GRCh38
NC_000003.11:g.133475740C= , CM000665.1:g.133475740C=	GRCh37
NC_000003.10:g.134958430C=	NCBI36
NG_013080.1:g.15764C=
NG_013080.2:g.99899C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.757C= MANE Select	ENSP00000385834.3:p.Pro253=
ENST00000402696.7:c.757C=	ENSP00000385834.3:p.Pro253=
ENST00000482271.5:c.376C=	ENSP00000419338.1:p.Pro126=
ENST00000485977.1:c.158-36C=	ENSP00000418716.1:n.158-36C=
NM_001063.3:c.757C=	NP_001054.1:p.Pro253=
XM_011513100.1:c.757C=	XP_011511402.1:p.Pro253=
NM_001354703.1:c.625C=	NP_001341632.1:p.Pro209=
NM_001354704.1:c.376C=	NP_001341633.1:p.Pro126=
NM_001063.4:c.757C= MANE Select	NP_001054.2:p.Pro253=
NM_001354703.2:c.625C=	NP_001341632.2:p.Pro209=
NM_001354704.2:c.376C=	NP_001341633.2:p.Pro126=