Canonical Allele Identifier: CA354611492

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133496060C>G (hg19) ; chr3:g.133777216C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777216C>G , CM000665.2:g.133777216C>G	GRCh38
NC_000003.11:g.133496060C>G , CM000665.1:g.133496060C>G	GRCh37
NC_000003.10:g.134978750C>G	NCBI36
NG_013080.1:g.36084C>G
NG_013080.2:g.120219C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.2040C>G MANE Select	ENSP00000385834.3:p.Asn680Lys
ENST00000402696.7:c.2040C>G	ENSP00000385834.3:p.Asn680Lys
ENST00000461695.1:c.771C>G
ENST00000467842.1:n.3034C>G
NM_001063.3:c.2040C>G	NP_001054.1:p.Asn680Lys
XM_011513100.1:c.2040C>G	XP_011511402.1:p.Asn680Lys
NM_001354703.1:c.1908C>G	NP_001341632.1:p.Asn636Lys
NM_001354704.1:c.1659C>G	NP_001341633.1:p.Asn553Lys
NM_001063.4:c.2040C>G MANE Select	NP_001054.2:p.Asn680Lys
NM_001354703.2:c.1908C>G	NP_001341632.2:p.Asn636Lys
NM_001354704.2:c.1659C>G	NP_001341633.2:p.Asn553Lys