Canonical Allele Identifier: CA354610305
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133775487T>A , CM000665.2:g.133775487T>A GRCh38
NC_000003.11:g.133494331T>A , CM000665.1:g.133494331T>A GRCh37
NC_000003.10:g.134977021T>A NCBI36
NG_013080.1:g.34355T>A
NG_013080.2:g.118490T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1742T>A MANE Select ENSP00000385834.3:p.Leu581Gln
ENST00000402696.7:c.1742T>A ENSP00000385834.3:p.Leu581Gln
ENST00000461695.1:c.473T>A
ENST00000467842.1:n.2736T>A
NM_001063.3:c.1742T>A NP_001054.1:p.Leu581Gln
XM_011513100.1:c.1742T>A XP_011511402.1:p.Leu581Gln
NM_001354703.1:c.1610T>A NP_001341632.1:p.Leu537Gln
NM_001354704.1:c.1361T>A NP_001341633.1:p.Leu454Gln
NM_001063.4:c.1742T>A MANE Select NP_001054.2:p.Leu581Gln
NM_001354703.2:c.1610T>A NP_001341632.2:p.Leu537Gln
NM_001354704.2:c.1361T>A NP_001341633.2:p.Leu454Gln