Canonical Allele Identifier: CA1403107598

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757124G= , CM000665.2:g.133757124G=	GRCh38
NC_000003.11:g.133475968G= , CM000665.1:g.133475968G=	GRCh37
NC_000003.10:g.134958658G=	NCBI36
NG_013080.1:g.15992G=
NG_013080.2:g.100127G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+115G= MANE Select	ENSP00000385834.3:n.870+115G=
ENST00000402696.7:c.870+115G=	ENSP00000385834.3:n.870+115G=
ENST00000485977.1:c.235+115G=	ENSP00000418716.1:n.235+115G=
NM_001063.3:c.870+115G=	NP_001054.1:n.870+115G=
XM_011513100.1:c.870+115G=	XP_011511402.1:n.870+115G=
NM_001354703.1:c.738+115G=	NP_001341632.1:n.738+115G=
NM_001354704.1:c.489+115G=	NP_001341633.1:n.489+115G=
NM_001063.4:c.870+115G= MANE Select	NP_001054.2:n.870+115G=
NM_001354703.2:c.738+115G=	NP_001341632.2:n.738+115G=
NM_001354704.2:c.489+115G=	NP_001341633.2:n.489+115G=