Canonical Allele Identifier: CA1403107393

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756959A= , CM000665.2:g.133756959A=	GRCh38
NC_000003.11:g.133475803A= , CM000665.1:g.133475803A=	GRCh37
NC_000003.10:g.134958493A=	NCBI36
NG_013080.1:g.15827A=
NG_013080.2:g.99962A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.820A= MANE Select	ENSP00000385834.3:p.Ser274=
ENST00000402696.7:c.820A=	ENSP00000385834.3:p.Ser274=
ENST00000485977.1:c.185A=	ENSP00000418716.1:p.Lys62=
NM_001063.3:c.820A=	NP_001054.1:p.Ser274=
XM_011513100.1:c.820A=	XP_011511402.1:p.Ser274=
NM_001354703.1:c.688A=	NP_001341632.1:p.Ser230=
NM_001354704.1:c.439A=	NP_001341633.1:p.Ser147=
NM_001063.4:c.820A= MANE Select	NP_001054.2:p.Ser274=
NM_001354703.2:c.688A=	NP_001341632.2:p.Ser230=
NM_001354704.2:c.439A=	NP_001341633.2:p.Ser147=