Canonical Allele Identifier: CA1403130772

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775473A= , CM000665.2:g.133775473A=	GRCh38
NC_000003.11:g.133494317A= , CM000665.1:g.133494317A=	GRCh37
NC_000003.10:g.134977007A=	NCBI36
NG_013080.1:g.34341A=
NG_013080.2:g.118476A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1728A= MANE Select	ENSP00000385834.3:p.Lys576=
ENST00000402696.7:c.1728A=	ENSP00000385834.3:p.Lys576=
ENST00000461695.1:c.459A=
ENST00000467842.1:n.2722A=
NM_001063.3:c.1728A=	NP_001054.1:p.Lys576=
XM_011513100.1:c.1728A=	XP_011511402.1:p.Lys576=
NM_001354703.1:c.1596A=	NP_001341632.1:p.Lys532=
NM_001354704.1:c.1347A=	NP_001341633.1:p.Lys449=
NM_001063.4:c.1728A= MANE Select	NP_001054.2:p.Lys576=
NM_001354703.2:c.1596A=	NP_001341632.2:p.Lys532=
NM_001354704.2:c.1347A=	NP_001341633.2:p.Lys449=