Canonical Allele Identifier: CA354610081

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494284C>G (hg19) ; chr3:g.133775440C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775440C>G , CM000665.2:g.133775440C>G	GRCh38
NC_000003.11:g.133494284C>G , CM000665.1:g.133494284C>G	GRCh37
NC_000003.10:g.134976974C>G	NCBI36
NG_013080.1:g.34308C>G
NG_013080.2:g.118443C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1695C>G MANE Select	ENSP00000385834.3:p.Asn565Lys
ENST00000402696.7:c.1695C>G	ENSP00000385834.3:p.Asn565Lys
ENST00000461695.1:c.426C>G
ENST00000467842.1:n.2689C>G
NM_001063.3:c.1695C>G	NP_001054.1:p.Asn565Lys
XM_011513100.1:c.1695C>G	XP_011511402.1:p.Asn565Lys
NM_001354703.1:c.1563C>G	NP_001341632.1:p.Asn521Lys
NM_001354704.1:c.1314C>G	NP_001341633.1:p.Asn438Lys
NM_001063.4:c.1695C>G MANE Select	NP_001054.2:p.Asn565Lys
NM_001354703.2:c.1563C>G	NP_001341632.2:p.Asn521Lys
NM_001354704.2:c.1314C>G	NP_001341633.2:p.Asn438Lys