Canonical Allele Identifier: CA1403107667

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757178A= , CM000665.2:g.133757178A=	GRCh38
NC_000003.11:g.133476022A= , CM000665.1:g.133476022A=	GRCh37
NC_000003.10:g.134958712A=	NCBI36
NG_013080.1:g.16046A=
NG_013080.2:g.100181A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+169A= MANE Select	ENSP00000385834.3:n.870+169A=
ENST00000402696.7:c.870+169A=	ENSP00000385834.3:n.870+169A=
ENST00000485977.1:c.235+169A=	ENSP00000418716.1:n.235+169A=
NM_001063.3:c.870+169A=	NP_001054.1:n.870+169A=
XM_011513100.1:c.870+169A=	XP_011511402.1:n.870+169A=
NM_001354703.1:c.738+169A=	NP_001341632.1:n.738+169A=
NM_001354704.1:c.489+169A=	NP_001341633.1:n.489+169A=
NM_001063.4:c.870+169A= MANE Select	NP_001054.2:n.870+169A=
NM_001354703.2:c.738+169A=	NP_001341632.2:n.738+169A=
NM_001354704.2:c.489+169A=	NP_001341633.2:n.489+169A=