Canonical Allele Identifier: CA1403107458

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756992C= , CM000665.2:g.133756992C=	GRCh38
NC_000003.11:g.133475836C= , CM000665.1:g.133475836C=	GRCh37
NC_000003.10:g.134958526C=	NCBI36
NG_013080.1:g.15860C=
NG_013080.2:g.99995C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.853C= MANE Select	ENSP00000385834.3:p.Leu285=
ENST00000402696.7:c.853C=	ENSP00000385834.3:p.Leu285=
ENST00000485977.1:c.218C=	ENSP00000418716.1:p.Ala73=
NM_001063.3:c.853C=	NP_001054.1:p.Leu285=
XM_011513100.1:c.853C=	XP_011511402.1:p.Leu285=
NM_001354703.1:c.721C=	NP_001341632.1:p.Leu241=
NM_001354704.1:c.472C=	NP_001341633.1:p.Leu158=
NM_001063.4:c.853C= MANE Select	NP_001054.2:p.Leu285=
NM_001354703.2:c.721C=	NP_001341632.2:p.Leu241=
NM_001354704.2:c.472C=	NP_001341633.2:p.Leu158=