Canonical Allele Identifier: CA435815832

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494347C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775503C>G , CM000665.2:g.133775503C>G	GRCh38
NC_000003.11:g.133494347C>G , CM000665.1:g.133494347C>G	GRCh37
NC_000003.10:g.134977037C>G	NCBI36
NG_013080.1:g.34371C>G
NG_013080.2:g.118506C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1758C>G MANE Select	ENSP00000385834.3:p.Thr586=
ENST00000402696.7:c.1758C>G	ENSP00000385834.3:p.Thr586=
ENST00000461695.1:c.489C>G
ENST00000467842.1:n.2752C>G
NM_001063.3:c.1758C>G	NP_001054.1:p.Thr586=
XM_011513100.1:c.1758C>G	XP_011511402.1:p.Thr586=
NM_001354703.1:c.1626C>G	NP_001341632.1:p.Thr542=
NM_001354704.1:c.1377C>G	NP_001341633.1:p.Thr459=
NM_001063.4:c.1758C>G MANE Select	NP_001054.2:p.Thr586=
NM_001354703.2:c.1626C>G	NP_001341632.2:p.Thr542=
NM_001354704.2:c.1377C>G	NP_001341633.2:p.Thr459=