Canonical Allele Identifier: CA1403107484

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757003G= , CM000665.2:g.133757003G=	GRCh38
NC_000003.11:g.133475847G= , CM000665.1:g.133475847G=	GRCh37
NC_000003.10:g.134958537G=	NCBI36
NG_013080.1:g.15871G=
NG_013080.2:g.100006G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.864G= MANE Select	ENSP00000385834.3:p.Gln288=
ENST00000402696.7:c.864G=	ENSP00000385834.3:p.Gln288=
ENST00000485977.1:c.229G=	ENSP00000418716.1:p.Gly77=
NM_001063.3:c.864G=	NP_001054.1:p.Gln288=
XM_011513100.1:c.864G=	XP_011511402.1:p.Gln288=
NM_001354703.1:c.732G=	NP_001341632.1:p.Gln244=
NM_001354704.1:c.483G=	NP_001341633.1:p.Gln161=
NM_001063.4:c.864G= MANE Select	NP_001054.2:p.Gln288=
NM_001354703.2:c.732G=	NP_001341632.2:p.Gln244=
NM_001354704.2:c.483G=	NP_001341633.2:p.Gln161=