Canonical Allele Identifier: CA353698099
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259965C>A , CM000665.2:g.87259965C>A GRCh38
NC_000003.11:g.87309115C>A , CM000665.1:g.87309115C>A GRCh37
NC_000003.10:g.87391805C>A NCBI36
NG_008225.2:g.21623G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.883G>T ENSP00000342931.3:p.Glu295Ter
ENST00000350375.7:c.805G>T MANE Select ENSP00000263781.2:p.Glu269Ter
ENST00000344265.7:c.883G>T ENSP00000342931.3:p.Glu295Ter
ENST00000350375.6:c.805G>T ENSP00000263781.2:p.Glu269Ter
ENST00000560656.1:c.579G>T ENSP00000452610.1:n.579G>T
ENST00000561167.5:c.580G>T ENSP00000454072.1:p.Glu194Ter
NM_000306.3:c.805G>T NP_000297.1:p.Glu269Ter
NM_001122757.2:c.883G>T NP_001116229.1:p.Glu295Ter
NM_000306.4:c.805G>T MANE Select NP_000297.1:p.Glu269Ter
NM_001122757.3:c.883G>T NP_001116229.1:p.Glu295Ter