Canonical Allele Identifier: CA354604845
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133756911A>G , CM000665.2:g.133756911A>G GRCh38
NC_000003.11:g.133475755A>G , CM000665.1:g.133475755A>G GRCh37
NC_000003.10:g.134958445A>G NCBI36
NG_013080.1:g.15779A>G
NG_013080.2:g.99914A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.772A>G MANE Select ENSP00000385834.3:p.Lys258Glu
ENST00000402696.7:c.772A>G ENSP00000385834.3:p.Lys258Glu
ENST00000482271.5:c.391A>G ENSP00000419338.1:p.Lys131Glu
ENST00000485977.1:c.158-21A>G ENSP00000418716.1:n.158-21A>G
NM_001063.3:c.772A>G NP_001054.1:p.Lys258Glu
XM_011513100.1:c.772A>G XP_011511402.1:p.Lys258Glu
NM_001354703.1:c.640A>G NP_001341632.1:p.Lys214Glu
NM_001354704.1:c.391A>G NP_001341633.1:p.Lys131Glu
NM_001063.4:c.772A>G MANE Select NP_001054.2:p.Lys258Glu
NM_001354703.2:c.640A>G NP_001341632.2:p.Lys214Glu
NM_001354704.2:c.391A>G NP_001341633.2:p.Lys131Glu