Canonical Allele Identifier: CA354611369

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133496006C>A (hg19) ; chr3:g.133777162C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777162C>A , CM000665.2:g.133777162C>A	GRCh38
NC_000003.11:g.133496006C>A , CM000665.1:g.133496006C>A	GRCh37
NC_000003.10:g.134978696C>A	NCBI36
NG_013080.1:g.36030C>A
NG_013080.2:g.120165C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1986C>A MANE Select	ENSP00000385834.3:p.Asp662Glu
ENST00000402696.7:c.1986C>A	ENSP00000385834.3:p.Asp662Glu
ENST00000461695.1:c.717C>A
ENST00000467842.1:n.2980C>A
NM_001063.3:c.1986C>A	NP_001054.1:p.Asp662Glu
XM_011513100.1:c.1986C>A	XP_011511402.1:p.Asp662Glu
NM_001354703.1:c.1854C>A	NP_001341632.1:p.Asp618Glu
NM_001354704.1:c.1605C>A	NP_001341633.1:p.Asp535Glu
NM_001063.4:c.1986C>A MANE Select	NP_001054.2:p.Asp662Glu
NM_001354703.2:c.1854C>A	NP_001341632.2:p.Asp618Glu
NM_001354704.2:c.1605C>A	NP_001341633.2:p.Asp535Glu