Canonical Allele Identifier: CA354610076
Gene: TF HGNC NCBI

Linked Data

dbSNP Id: rs1326236551

Genomic Alleles

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

Transcript Alleles

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