Canonical Allele Identifier: CA1403130745

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775446T= , CM000665.2:g.133775446T=	GRCh38
NC_000003.11:g.133494290T= , CM000665.1:g.133494290T=	GRCh37
NC_000003.10:g.134976980T=	NCBI36
NG_013080.1:g.34314T=
NG_013080.2:g.118449T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1701T= MANE Select	ENSP00000385834.3:p.Asp567=
ENST00000402696.7:c.1701T=	ENSP00000385834.3:p.Asp567=
ENST00000461695.1:c.432T=
ENST00000467842.1:n.2695T=
NM_001063.3:c.1701T=	NP_001054.1:p.Asp567=
XM_011513100.1:c.1701T=	XP_011511402.1:p.Asp567=
NM_001354703.1:c.1569T=	NP_001341632.1:p.Asp523=
NM_001354704.1:c.1320T=	NP_001341633.1:p.Asp440=
NM_001063.4:c.1701T= MANE Select	NP_001054.2:p.Asp567=
NM_001354703.2:c.1569T=	NP_001341632.2:p.Asp523=
NM_001354704.2:c.1320T=	NP_001341633.2:p.Asp440=