Canonical Allele Identifier: CA122559

Gene: TF

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_001063.4:c.956A>G MANE Select	NP_001054.2:p.His319Arg
ENST00000402696.9:c.956A>G MANE Select	ENSP00000385834.3:p.His319Arg
NM_001063.3:c.956A>G	NP_001054.1:p.His319Arg
NM_001354703.1:c.824A>G	NP_001341632.1:p.His275Arg
NM_001354703.2:c.824A>G	NP_001341632.2:p.His275Arg
NM_001354704.1:c.575A>G	NP_001341633.1:p.His192Arg
NM_001354704.2:c.575A>G	NP_001341633.2:p.His192Arg
ENST00000402696.7:c.956A>G	ENSP00000385834.3:p.His319Arg
ENST00000485977.1:c.*12A>G	ENSP00000418716.1:n.*12A>G
XM_011513100.1:c.956A>G	XP_011511402.1:p.His319Arg