Canonical Allele Identifier: CA1381535039
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264335T= , CM000665.2:g.87264335T= GRCh38
NC_000003.11:g.87313485T= , CM000665.1:g.87313485T= GRCh37
NC_000003.10:g.87396175T= NCBI36
NG_008225.2:g.17253A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.470A= ENSP00000342931.3:p.Glu157=
ENST00000350375.7:c.392A= MANE Select ENSP00000263781.2:p.Glu131=
ENST00000344265.7:c.470A= ENSP00000342931.3:p.Glu157=
ENST00000350375.6:c.392A= ENSP00000263781.2:p.Glu131=
ENST00000560656.1:c.392A= ENSP00000452610.1:p.Glu131=
ENST00000561167.5:c.215-2100A= ENSP00000454072.1:n.215-2100A=
NM_000306.3:c.392A= NP_000297.1:p.Glu131=
NM_001122757.2:c.470A= NP_001116229.1:p.Glu157=
NM_000306.4:c.392A= MANE Select NP_000297.1:p.Glu131=
NM_001122757.3:c.470A= NP_001116229.1:p.Glu157=