Canonical Allele Identifier: CA1403108522

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757854A= , CM000665.2:g.133757854A=	GRCh38
NC_000003.11:g.133476698A= , CM000665.1:g.133476698A=	GRCh37
NC_000003.10:g.134959388A=	NCBI36
NG_013080.1:g.16722A=
NG_013080.2:g.100857A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001063.4:c.956A= MANE Select	NP_001054.2:p.His319=
ENST00000402696.9:c.956A= MANE Select	ENSP00000385834.3:p.His319=
NM_001063.3:c.956A=	NP_001054.1:p.His319=
NM_001354703.1:c.824A=	NP_001341632.1:p.His275=
NM_001354703.2:c.824A=	NP_001341632.2:p.His275=
NM_001354704.1:c.575A=	NP_001341633.1:p.His192=
NM_001354704.2:c.575A=	NP_001341633.2:p.His192=
ENST00000402696.7:c.956A=	ENSP00000385834.3:p.His319=
ENST00000485977.1:c.*12A=	ENSP00000418716.1:n.*12A=
XM_011513100.1:c.956A=	XP_011511402.1:p.His319=