Canonical Allele Identifier: CA1403118136

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133765185G= , CM000665.2:g.133765185G=	GRCh38
NC_000003.11:g.133484029G= , CM000665.1:g.133484029G=	GRCh37
NC_000003.10:g.134966719G=	NCBI36
NG_013080.1:g.24053G=
NG_013080.2:g.108188G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1330+278G= MANE Select	ENSP00000385834.3:n.1330+278G=
ENST00000402696.7:c.1330+278G=	ENSP00000385834.3:n.1330+278G=
NM_001063.3:c.1330+278G=	NP_001054.1:n.1330+278G=
XM_011513100.1:c.1330+278G=	XP_011511402.1:n.1330+278G=
NM_001354703.1:c.1198+278G=	NP_001341632.1:n.1198+278G=
NM_001354704.1:c.949+278G=	NP_001341633.1:n.949+278G=
NM_001063.4:c.1330+278G= MANE Select	NP_001054.2:n.1330+278G=
NM_001354703.2:c.1198+278G=	NP_001341632.2:n.1198+278G=
NM_001354704.2:c.949+278G=	NP_001341633.2:n.949+278G=