Canonical Allele Identifier: CA1403124845

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777112A= , CM000665.2:g.133777112A=	GRCh38
NC_000003.11:g.133495956A= , CM000665.1:g.133495956A=	GRCh37
NC_000003.10:g.134978646A=	NCBI36
NG_013080.1:g.35980A=
NG_013080.2:g.120115A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001063.4:c.1936A= MANE Select	NP_001054.2:p.Lys646=
ENST00000402696.9:c.1936A= MANE Select	ENSP00000385834.3:p.Lys646=
NM_001063.3:c.1936A=	NP_001054.1:p.Lys646=
NM_001354703.1:c.1804A=	NP_001341632.1:p.Lys602=
NM_001354703.2:c.1804A=	NP_001341632.2:p.Lys602=
NM_001354704.1:c.1555A=	NP_001341633.1:p.Lys519=
NM_001354704.2:c.1555A=	NP_001341633.2:p.Lys519=
ENST00000402696.7:c.1936A=	ENSP00000385834.3:p.Lys646=
ENST00000461695.1:c.667A=
ENST00000467842.1:n.2930A=
XM_011513100.1:c.1936A=	XP_011511402.1:p.Lys646=