Canonical Allele Identifier: CA1403122947

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775605A= , CM000665.2:g.133775605A=	GRCh38
NC_000003.11:g.133494449A= , CM000665.1:g.133494449A=	GRCh37
NC_000003.10:g.134977139A=	NCBI36
NG_013080.1:g.34473A=
NG_013080.2:g.118608A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1860A= MANE Select	ENSP00000385834.3:p.Leu620=
ENST00000402696.7:c.1860A=	ENSP00000385834.3:p.Leu620=
ENST00000461695.1:c.591A=
ENST00000467842.1:n.2854A=
NM_001063.3:c.1860A=	NP_001054.1:p.Leu620=
XM_011513100.1:c.1860A=	XP_011511402.1:p.Leu620=
NM_001354703.1:c.1728A=	NP_001341632.1:p.Leu576=
NM_001354704.1:c.1479A=	NP_001341633.1:p.Leu493=
NM_001063.4:c.1860A= MANE Select	NP_001054.2:p.Leu620=
NM_001354703.2:c.1728A=	NP_001341632.2:p.Leu576=
NM_001354704.2:c.1479A=	NP_001341633.2:p.Leu493=