Canonical Allele Identifier: CA1403107389

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756957G= , CM000665.2:g.133756957G=	GRCh38
NC_000003.11:g.133475801G= , CM000665.1:g.133475801G=	GRCh37
NC_000003.10:g.134958491G=	NCBI36
NG_013080.1:g.15825G=
NG_013080.2:g.99960G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.818G= MANE Select	ENSP00000385834.3:p.Arg273=
ENST00000402696.7:c.818G=	ENSP00000385834.3:p.Arg273=
ENST00000485977.1:c.183G=	ENSP00000418716.1:p.Pro61=
NM_001063.3:c.818G=	NP_001054.1:p.Arg273=
XM_011513100.1:c.818G=	XP_011511402.1:p.Arg273=
NM_001354703.1:c.686G=	NP_001341632.1:p.Arg229=
NM_001354704.1:c.437G=	NP_001341633.1:p.Arg146=
NM_001063.4:c.818G= MANE Select	NP_001054.2:p.Arg273=
NM_001354703.2:c.686G=	NP_001341632.2:p.Arg229=
NM_001354704.2:c.437G=	NP_001341633.2:p.Arg146=