Canonical Allele Identifier: CA354610288

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494327T>A (hg19) ; chr3:g.133775483T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775483T>A , CM000665.2:g.133775483T>A	GRCh38
NC_000003.11:g.133494327T>A , CM000665.1:g.133494327T>A	GRCh37
NC_000003.10:g.134977017T>A	NCBI36
NG_013080.1:g.34351T>A
NG_013080.2:g.118486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1738T>A MANE Select	ENSP00000385834.3:p.Leu580Met
ENST00000402696.7:c.1738T>A	ENSP00000385834.3:p.Leu580Met
ENST00000461695.1:c.469T>A
ENST00000467842.1:n.2732T>A
NM_001063.3:c.1738T>A	NP_001054.1:p.Leu580Met
XM_011513100.1:c.1738T>A	XP_011511402.1:p.Leu580Met
NM_001354703.1:c.1606T>A	NP_001341632.1:p.Leu536Met
NM_001354704.1:c.1357T>A	NP_001341633.1:p.Leu453Met
NM_001063.4:c.1738T>A MANE Select	NP_001054.2:p.Leu580Met
NM_001354703.2:c.1606T>A	NP_001341632.2:p.Leu536Met
NM_001354704.2:c.1357T>A	NP_001341633.2:p.Leu453Met