Canonical Allele Identifier: CA1403107258

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756894A= , CM000665.2:g.133756894A=	GRCh38
NC_000003.11:g.133475738A= , CM000665.1:g.133475738A=	GRCh37
NC_000003.10:g.134958428A=	NCBI36
NG_013080.1:g.15762A=
NG_013080.2:g.99897A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.755A= MANE Select	ENSP00000385834.3:p.Lys252=
ENST00000402696.7:c.755A=	ENSP00000385834.3:p.Lys252=
ENST00000482271.5:c.374A=	ENSP00000419338.1:p.Lys125=
ENST00000485977.1:c.158-38A=	ENSP00000418716.1:n.158-38A=
NM_001063.3:c.755A=	NP_001054.1:p.Lys252=
XM_011513100.1:c.755A=	XP_011511402.1:p.Lys252=
NM_001354703.1:c.623A=	NP_001341632.1:p.Lys208=
NM_001354704.1:c.374A=	NP_001341633.1:p.Lys125=
NM_001063.4:c.755A= MANE Select	NP_001054.2:p.Lys252=
NM_001354703.2:c.623A=	NP_001341632.2:p.Lys208=
NM_001354704.2:c.374A=	NP_001341633.2:p.Lys125=