Canonical Allele Identifier: CA1403124997

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777188G= , CM000665.2:g.133777188G=	GRCh38
NC_000003.11:g.133496032G= , CM000665.1:g.133496032G=	GRCh37
NC_000003.10:g.134978722G=	NCBI36
NG_013080.1:g.36056G=
NG_013080.2:g.120191G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001063.4:c.2012G= MANE Select	NP_001054.2:p.Gly671=
ENST00000402696.9:c.2012G= MANE Select	ENSP00000385834.3:p.Gly671=
NM_001063.3:c.2012G=	NP_001054.1:p.Gly671=
NM_001354703.1:c.1880G=	NP_001341632.1:p.Gly627=
NM_001354703.2:c.1880G=	NP_001341632.2:p.Gly627=
NM_001354704.1:c.1631G=	NP_001341633.1:p.Gly544=
NM_001354704.2:c.1631G=	NP_001341633.2:p.Gly544=
ENST00000402696.7:c.2012G=	ENSP00000385834.3:p.Gly671=
ENST00000461695.1:c.743G=
ENST00000467842.1:n.3006G=
XM_011513100.1:c.2012G=	XP_011511402.1:p.Gly671=