Canonical Allele Identifier: CA1403107671

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757180G= , CM000665.2:g.133757180G=	GRCh38
NC_000003.11:g.133476024G= , CM000665.1:g.133476024G=	GRCh37
NC_000003.10:g.134958714G=	NCBI36
NG_013080.1:g.16048G=
NG_013080.2:g.100183G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+171G= MANE Select	ENSP00000385834.3:n.870+171G=
ENST00000402696.7:c.870+171G=	ENSP00000385834.3:n.870+171G=
ENST00000485977.1:c.235+171G=	ENSP00000418716.1:n.235+171G=
NM_001063.3:c.870+171G=	NP_001054.1:n.870+171G=
XM_011513100.1:c.870+171G=	XP_011511402.1:n.870+171G=
NM_001354703.1:c.738+171G=	NP_001341632.1:n.738+171G=
NM_001354704.1:c.489+171G=	NP_001341633.1:n.489+171G=
NM_001063.4:c.870+171G= MANE Select	NP_001054.2:n.870+171G=
NM_001354703.2:c.738+171G=	NP_001341632.2:n.738+171G=
NM_001354704.2:c.489+171G=	NP_001341633.2:n.489+171G=