Canonical Allele Identifier: CA1403124899

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777137C= , CM000665.2:g.133777137C=	GRCh38
NC_000003.11:g.133495981C= , CM000665.1:g.133495981C=	GRCh37
NC_000003.10:g.134978671C=	NCBI36
NG_013080.1:g.36005C=
NG_013080.2:g.120140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1961C= MANE Select	ENSP00000385834.3:p.Thr654=
ENST00000402696.7:c.1961C=	ENSP00000385834.3:p.Thr654=
ENST00000461695.1:c.692C=
ENST00000467842.1:n.2955C=
NM_001063.3:c.1961C=	NP_001054.1:p.Thr654=
XM_011513100.1:c.1961C=	XP_011511402.1:p.Thr654=
NM_001354703.1:c.1829C=	NP_001341632.1:p.Thr610=
NM_001354704.1:c.1580C=	NP_001341633.1:p.Thr527=
NM_001063.4:c.1961C= MANE Select	NP_001054.2:p.Thr654=
NM_001354703.2:c.1829C=	NP_001341632.2:p.Thr610=
NM_001354704.2:c.1580C=	NP_001341633.2:p.Thr527=