Canonical Allele Identifier: CA354610331

Gene: TF

Linked Data

• COSMIC: COSM5734686
• MyVariant Identifiers: chr3:g.133494343G>A (hg19) ; chr3:g.133775499G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775499G>A , CM000665.2:g.133775499G>A	GRCh38
NC_000003.11:g.133494343G>A , CM000665.1:g.133494343G>A	GRCh37
NC_000003.10:g.134977033G>A	NCBI36
NG_013080.1:g.34367G>A
NG_013080.2:g.118502G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1754G>A MANE Select	ENSP00000385834.3:p.Gly585Asp
ENST00000402696.7:c.1754G>A	ENSP00000385834.3:p.Gly585Asp
ENST00000461695.1:c.485G>A
ENST00000467842.1:n.2748G>A
NM_001063.3:c.1754G>A	NP_001054.1:p.Gly585Asp
XM_011513100.1:c.1754G>A	XP_011511402.1:p.Gly585Asp
NM_001354703.1:c.1622G>A	NP_001341632.1:p.Gly541Asp
NM_001354704.1:c.1373G>A	NP_001341633.1:p.Gly458Asp
NM_001063.4:c.1754G>A MANE Select	NP_001054.2:p.Gly585Asp
NM_001354703.2:c.1622G>A	NP_001341632.2:p.Gly541Asp
NM_001354704.2:c.1373G>A	NP_001341633.2:p.Gly458Asp