Canonical Allele Identifier: CA1403122966

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775608T= , CM000665.2:g.133775608T=	GRCh38
NC_000003.11:g.133494452T= , CM000665.1:g.133494452T=	GRCh37
NC_000003.10:g.134977142T=	NCBI36
NG_013080.1:g.34476T=
NG_013080.2:g.118611T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1863T= MANE Select	ENSP00000385834.3:p.Arg621=
ENST00000402696.7:c.1863T=	ENSP00000385834.3:p.Arg621=
ENST00000461695.1:c.594T=
ENST00000467842.1:n.2857T=
NM_001063.3:c.1863T=	NP_001054.1:p.Arg621=
XM_011513100.1:c.1863T=	XP_011511402.1:p.Arg621=
NM_001354703.1:c.1731T=	NP_001341632.1:p.Arg577=
NM_001354704.1:c.1482T=	NP_001341633.1:p.Arg494=
NM_001063.4:c.1863T= MANE Select	NP_001054.2:p.Arg621=
NM_001354703.2:c.1731T=	NP_001341632.2:p.Arg577=
NM_001354704.2:c.1482T=	NP_001341633.2:p.Arg494=