Canonical Allele Identifier: CA1403130728

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775435A= , CM000665.2:g.133775435A=	GRCh38
NC_000003.11:g.133494279A= , CM000665.1:g.133494279A=	GRCh37
NC_000003.10:g.134976969A=	NCBI36
NG_013080.1:g.34303A=
NG_013080.2:g.118438A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1690A= MANE Select	ENSP00000385834.3:p.Lys564=
ENST00000402696.7:c.1690A=	ENSP00000385834.3:p.Lys564=
ENST00000461695.1:c.421A=
ENST00000467842.1:n.2684A=
NM_001063.3:c.1690A=	NP_001054.1:p.Lys564=
XM_011513100.1:c.1690A=	XP_011511402.1:p.Lys564=
NM_001354703.1:c.1558A=	NP_001341632.1:p.Lys520=
NM_001354704.1:c.1309A=	NP_001341633.1:p.Lys437=
NM_001063.4:c.1690A= MANE Select	NP_001054.2:p.Lys564=
NM_001354703.2:c.1558A=	NP_001341632.2:p.Lys520=
NM_001354704.2:c.1309A=	NP_001341633.2:p.Lys437=