Canonical Allele Identifier: CA1403130776

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775479T= , CM000665.2:g.133775479T=	GRCh38
NC_000003.11:g.133494323T= , CM000665.1:g.133494323T=	GRCh37
NC_000003.10:g.134977013T=	NCBI36
NG_013080.1:g.34347T=
NG_013080.2:g.118482T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1734T= MANE Select	ENSP00000385834.3:p.Tyr578=
ENST00000402696.7:c.1734T=	ENSP00000385834.3:p.Tyr578=
ENST00000461695.1:c.465T=
ENST00000467842.1:n.2728T=
NM_001063.3:c.1734T=	NP_001054.1:p.Tyr578=
XM_011513100.1:c.1734T=	XP_011511402.1:p.Tyr578=
NM_001354703.1:c.1602T=	NP_001341632.1:p.Tyr534=
NM_001354704.1:c.1353T=	NP_001341633.1:p.Tyr451=
NM_001063.4:c.1734T= MANE Select	NP_001054.2:p.Tyr578=
NM_001354703.2:c.1602T=	NP_001341632.2:p.Tyr534=
NM_001354704.2:c.1353T=	NP_001341633.2:p.Tyr451=