Canonical Allele Identifier: CA1403122791

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775532G= , CM000665.2:g.133775532G=	GRCh38
NC_000003.11:g.133494376G= , CM000665.1:g.133494376G=	GRCh37
NC_000003.10:g.134977066G=	NCBI36
NG_013080.1:g.34400G=
NG_013080.2:g.118535G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1787G= MANE Select	ENSP00000385834.3:p.Cys596=
ENST00000402696.7:c.1787G=	ENSP00000385834.3:p.Cys596=
ENST00000461695.1:c.518G=
ENST00000467842.1:n.2781G=
NM_001063.3:c.1787G=	NP_001054.1:p.Cys596=
XM_011513100.1:c.1787G=	XP_011511402.1:p.Cys596=
NM_001354703.1:c.1655G=	NP_001341632.1:p.Cys552=
NM_001354704.1:c.1406G=	NP_001341633.1:p.Cys469=
NM_001063.4:c.1787G= MANE Select	NP_001054.2:p.Cys596=
NM_001354703.2:c.1655G=	NP_001341632.2:p.Cys552=
NM_001354704.2:c.1406G=	NP_001341633.2:p.Cys469=