Canonical Allele Identifier: CA354604843

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475754C>G (hg19) ; chr3:g.133756910C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756910C>G , CM000665.2:g.133756910C>G	GRCh38
NC_000003.11:g.133475754C>G , CM000665.1:g.133475754C>G	GRCh37
NC_000003.10:g.134958444C>G	NCBI36
NG_013080.1:g.15778C>G
NG_013080.2:g.99913C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.771C>G MANE Select	ENSP00000385834.3:p.Tyr257Ter
ENST00000402696.7:c.771C>G	ENSP00000385834.3:p.Tyr257Ter
ENST00000482271.5:c.390C>G	ENSP00000419338.1:p.Tyr130Ter
ENST00000485977.1:c.158-22C>G	ENSP00000418716.1:n.158-22C>G
NM_001063.3:c.771C>G	NP_001054.1:p.Tyr257Ter
XM_011513100.1:c.771C>G	XP_011511402.1:p.Tyr257Ter
NM_001354703.1:c.639C>G	NP_001341632.1:p.Tyr213Ter
NM_001354704.1:c.390C>G	NP_001341633.1:p.Tyr130Ter
NM_001063.4:c.771C>G MANE Select	NP_001054.2:p.Tyr257Ter
NM_001354703.2:c.639C>G	NP_001341632.2:p.Tyr213Ter
NM_001354704.2:c.390C>G	NP_001341633.2:p.Tyr130Ter