Canonical Allele Identifier: CA1403122747

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775520A= , CM000665.2:g.133775520A=	GRCh38
NC_000003.11:g.133494364A= , CM000665.1:g.133494364A=	GRCh37
NC_000003.10:g.134977054A=	NCBI36
NG_013080.1:g.34388A=
NG_013080.2:g.118523A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1775A= MANE Select	ENSP00000385834.3:p.Glu592=
ENST00000402696.7:c.1775A=	ENSP00000385834.3:p.Glu592=
ENST00000461695.1:c.506A=
ENST00000467842.1:n.2769A=
NM_001063.3:c.1775A=	NP_001054.1:p.Glu592=
XM_011513100.1:c.1775A=	XP_011511402.1:p.Glu592=
NM_001354703.1:c.1643A=	NP_001341632.1:p.Glu548=
NM_001354704.1:c.1394A=	NP_001341633.1:p.Glu465=
NM_001063.4:c.1775A= MANE Select	NP_001054.2:p.Glu592=
NM_001354703.2:c.1643A=	NP_001341632.2:p.Glu548=
NM_001354704.2:c.1394A=	NP_001341633.2:p.Glu465=