Canonical Allele Identifier: CA1403119475

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766395T= , CM000665.2:g.133766395T=	GRCh38
NC_000003.11:g.133485239T= , CM000665.1:g.133485239T=	GRCh37
NC_000003.10:g.134967929T=	NCBI36
NG_013080.1:g.25263T=
NG_013080.2:g.109398T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1448T= MANE Select	ENSP00000385834.3:p.Met483=
ENST00000402696.7:c.1448T=	ENSP00000385834.3:p.Met483=
ENST00000461695.1:c.118T=
NM_001063.3:c.1448T=	NP_001054.1:p.Met483=
XM_011513100.1:c.1448T=	XP_011511402.1:p.Met483=
NM_001354703.1:c.1316T=	NP_001341632.1:p.Met439=
NM_001354704.1:c.1067T=	NP_001341633.1:p.Met356=
NM_001063.4:c.1448T= MANE Select	NP_001054.2:p.Met483=
NM_001354703.2:c.1316T=	NP_001341632.2:p.Met439=
NM_001354704.2:c.1067T=	NP_001341633.2:p.Met356=