Canonical Allele Identifier: CA1403107453

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756990A= , CM000665.2:g.133756990A=	GRCh38
NC_000003.11:g.133475834A= , CM000665.1:g.133475834A=	GRCh37
NC_000003.10:g.134958524A=	NCBI36
NG_013080.1:g.15858A=
NG_013080.2:g.99993A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.851A= MANE Select	ENSP00000385834.3:p.Glu284=
ENST00000402696.7:c.851A=	ENSP00000385834.3:p.Glu284=
ENST00000485977.1:c.216A=	ENSP00000418716.1:p.Gly72=
NM_001063.3:c.851A=	NP_001054.1:p.Glu284=
XM_011513100.1:c.851A=	XP_011511402.1:p.Glu284=
NM_001354703.1:c.719A=	NP_001341632.1:p.Glu240=
NM_001354704.1:c.470A=	NP_001341633.1:p.Glu157=
NM_001063.4:c.851A= MANE Select	NP_001054.2:p.Glu284=
NM_001354703.2:c.719A=	NP_001341632.2:p.Glu240=
NM_001354704.2:c.470A=	NP_001341633.2:p.Glu157=