Canonical Allele Identifier: CA1403122884

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775570C= , CM000665.2:g.133775570C=	GRCh38
NC_000003.11:g.133494414C= , CM000665.1:g.133494414C=	GRCh37
NC_000003.10:g.134977104C=	NCBI36
NG_013080.1:g.34438C=
NG_013080.2:g.118573C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001063.4:c.1825C= MANE Select	NP_001054.2:p.Arg609=
ENST00000402696.9:c.1825C= MANE Select	ENSP00000385834.3:p.Arg609=
NM_001063.3:c.1825C=	NP_001054.1:p.Arg609=
NM_001354703.1:c.1693C=	NP_001341632.1:p.Arg565=
NM_001354703.2:c.1693C=	NP_001341632.2:p.Arg565=
NM_001354704.1:c.1444C=	NP_001341633.1:p.Arg482=
NM_001354704.2:c.1444C=	NP_001341633.2:p.Arg482=
ENST00000402696.7:c.1825C=	ENSP00000385834.3:p.Arg609=
ENST00000461695.1:c.556C=
ENST00000467842.1:n.2819C=
XM_011513100.1:c.1825C=	XP_011511402.1:p.Arg609=