Canonical Allele Identifier: CA1403130766

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775463T= , CM000665.2:g.133775463T=	GRCh38
NC_000003.11:g.133494307T= , CM000665.1:g.133494307T=	GRCh37
NC_000003.10:g.134976997T=	NCBI36
NG_013080.1:g.34331T=
NG_013080.2:g.118466T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1718T= MANE Select	ENSP00000385834.3:p.Leu573=
ENST00000402696.7:c.1718T=	ENSP00000385834.3:p.Leu573=
ENST00000461695.1:c.449T=
ENST00000467842.1:n.2712T=
NM_001063.3:c.1718T=	NP_001054.1:p.Leu573=
XM_011513100.1:c.1718T=	XP_011511402.1:p.Leu573=
NM_001354703.1:c.1586T=	NP_001341632.1:p.Leu529=
NM_001354704.1:c.1337T=	NP_001341633.1:p.Leu446=
NM_001063.4:c.1718T= MANE Select	NP_001054.2:p.Leu573=
NM_001354703.2:c.1586T=	NP_001341632.2:p.Leu529=
NM_001354704.2:c.1337T=	NP_001341633.2:p.Leu446=