Canonical Allele Identifier: CA354610065
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133775438A>T , CM000665.2:g.133775438A>T GRCh38
NC_000003.11:g.133494282A>T , CM000665.1:g.133494282A>T GRCh37
NC_000003.10:g.134976972A>T NCBI36
NG_013080.1:g.34306A>T
NG_013080.2:g.118441A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1693A>T MANE Select ENSP00000385834.3:p.Asn565Tyr
ENST00000402696.7:c.1693A>T ENSP00000385834.3:p.Asn565Tyr
ENST00000461695.1:c.424A>T
ENST00000467842.1:n.2687A>T
NM_001063.3:c.1693A>T NP_001054.1:p.Asn565Tyr
XM_011513100.1:c.1693A>T XP_011511402.1:p.Asn565Tyr
NM_001354703.1:c.1561A>T NP_001341632.1:p.Asn521Tyr
NM_001354704.1:c.1312A>T NP_001341633.1:p.Asn438Tyr
NM_001063.4:c.1693A>T MANE Select NP_001054.2:p.Asn565Tyr
NM_001354703.2:c.1561A>T NP_001341632.2:p.Asn521Tyr
NM_001354704.2:c.1312A>T NP_001341633.2:p.Asn438Tyr