Canonical Allele Identifier: CA354604853
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133756914G>A , CM000665.2:g.133756914G>A GRCh38
NC_000003.11:g.133475758G>A , CM000665.1:g.133475758G>A GRCh37
NC_000003.10:g.134958448G>A NCBI36
NG_013080.1:g.15782G>A
NG_013080.2:g.99917G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.775G>A MANE Select ENSP00000385834.3:p.Asp259Asn
ENST00000402696.7:c.775G>A ENSP00000385834.3:p.Asp259Asn
ENST00000482271.5:c.394G>A ENSP00000419338.1:p.Asp132Asn
ENST00000485977.1:c.158-18G>A ENSP00000418716.1:n.158-18G>A
NM_001063.3:c.775G>A NP_001054.1:p.Asp259Asn
XM_011513100.1:c.775G>A XP_011511402.1:p.Asp259Asn
NM_001354703.1:c.643G>A NP_001341632.1:p.Asp215Asn
NM_001354704.1:c.394G>A NP_001341633.1:p.Asp132Asn
NM_001063.4:c.775G>A MANE Select NP_001054.2:p.Asp259Asn
NM_001354703.2:c.643G>A NP_001341632.2:p.Asp215Asn
NM_001354704.2:c.394G>A NP_001341633.2:p.Asp132Asn