Canonical Allele Identifier: CA434627036
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87313490G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264340G>A , CM000665.2:g.87264340G>A GRCh38
NC_000003.11:g.87313490G>A , CM000665.1:g.87313490G>A GRCh37
NC_000003.10:g.87396180G>A NCBI36
NG_008225.2:g.17248C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.465C>T ENSP00000342931.3:p.Ile155=
ENST00000350375.7:c.387C>T MANE Select ENSP00000263781.2:p.Ile129=
ENST00000344265.7:c.465C>T ENSP00000342931.3:p.Ile155=
ENST00000350375.6:c.387C>T ENSP00000263781.2:p.Ile129=
ENST00000560656.1:c.387C>T ENSP00000452610.1:p.Ile129=
ENST00000561167.5:c.215-2105C>T ENSP00000454072.1:n.215-2105C>T
NM_000306.3:c.387C>T NP_000297.1:p.Ile129=
NM_001122757.2:c.465C>T NP_001116229.1:p.Ile155=
NM_000306.4:c.387C>T MANE Select NP_000297.1:p.Ile129=
NM_001122757.3:c.465C>T NP_001116229.1:p.Ile155=