Canonical Allele Identifier: CA1403107582

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757106G= , CM000665.2:g.133757106G=	GRCh38
NC_000003.11:g.133475950G= , CM000665.1:g.133475950G=	GRCh37
NC_000003.10:g.134958640G=	NCBI36
NG_013080.1:g.15974G=
NG_013080.2:g.100109G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+97G= MANE Select	ENSP00000385834.3:n.870+97G=
ENST00000402696.7:c.870+97G=	ENSP00000385834.3:n.870+97G=
ENST00000485977.1:c.235+97G=	ENSP00000418716.1:n.235+97G=
NM_001063.3:c.870+97G=	NP_001054.1:n.870+97G=
XM_011513100.1:c.870+97G=	XP_011511402.1:n.870+97G=
NM_001354703.1:c.738+97G=	NP_001341632.1:n.738+97G=
NM_001354704.1:c.489+97G=	NP_001341633.1:n.489+97G=
NM_001063.4:c.870+97G= MANE Select	NP_001054.2:n.870+97G=
NM_001354703.2:c.738+97G=	NP_001341632.2:n.738+97G=
NM_001354704.2:c.489+97G=	NP_001341633.2:n.489+97G=