Canonical Allele Identifier: CA354604841
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133756909A>T , CM000665.2:g.133756909A>T GRCh38
NC_000003.11:g.133475753A>T , CM000665.1:g.133475753A>T GRCh37
NC_000003.10:g.134958443A>T NCBI36
NG_013080.1:g.15777A>T
NG_013080.2:g.99912A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.770A>T MANE Select ENSP00000385834.3:p.Tyr257Phe
ENST00000402696.7:c.770A>T ENSP00000385834.3:p.Tyr257Phe
ENST00000482271.5:c.389A>T ENSP00000419338.1:p.Tyr130Phe
ENST00000485977.1:c.158-23A>T ENSP00000418716.1:n.158-23A>T
NM_001063.3:c.770A>T NP_001054.1:p.Tyr257Phe
XM_011513100.1:c.770A>T XP_011511402.1:p.Tyr257Phe
NM_001354703.1:c.638A>T NP_001341632.1:p.Tyr213Phe
NM_001354704.1:c.389A>T NP_001341633.1:p.Tyr130Phe
NM_001063.4:c.770A>T MANE Select NP_001054.2:p.Tyr257Phe
NM_001354703.2:c.638A>T NP_001341632.2:p.Tyr213Phe
NM_001354704.2:c.389A>T NP_001341633.2:p.Tyr130Phe