Canonical Allele Identifier: CA354611378

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133496010A>G (hg19) ; chr3:g.133777166A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777166A>G , CM000665.2:g.133777166A>G	GRCh38
NC_000003.11:g.133496010A>G , CM000665.1:g.133496010A>G	GRCh37
NC_000003.10:g.134978700A>G	NCBI36
NG_013080.1:g.36034A>G
NG_013080.2:g.120169A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1990A>G MANE Select	ENSP00000385834.3:p.Asn664Asp
ENST00000402696.7:c.1990A>G	ENSP00000385834.3:p.Asn664Asp
ENST00000461695.1:c.721A>G
ENST00000467842.1:n.2984A>G
NM_001063.3:c.1990A>G	NP_001054.1:p.Asn664Asp
XM_011513100.1:c.1990A>G	XP_011511402.1:p.Asn664Asp
NM_001354703.1:c.1858A>G	NP_001341632.1:p.Asn620Asp
NM_001354704.1:c.1609A>G	NP_001341633.1:p.Asn537Asp
NM_001063.4:c.1990A>G MANE Select	NP_001054.2:p.Asn664Asp
NM_001354703.2:c.1858A>G	NP_001341632.2:p.Asn620Asp
NM_001354704.2:c.1609A>G	NP_001341633.2:p.Asn537Asp