Canonical Allele Identifier: CA434575741
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87311348A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262198A>C , CM000665.2:g.87262198A>C GRCh38
NC_000003.11:g.87311348A>C , CM000665.1:g.87311348A>C GRCh37
NC_000003.10:g.87394038A>C NCBI36
NG_008225.2:g.19390T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.555T>G ENSP00000342931.3:p.Ala185=
ENST00000350375.7:c.477T>G MANE Select ENSP00000263781.2:p.Ala159=
ENST00000344265.7:c.555T>G ENSP00000342931.3:p.Ala185=
ENST00000350375.6:c.477T>G ENSP00000263781.2:p.Ala159=
ENST00000560656.1:c.439+2090T>G ENSP00000452610.1:n.439+2090T>G
ENST00000561167.5:c.252T>G ENSP00000454072.1:p.Ala84=
NM_000306.3:c.477T>G NP_000297.1:p.Ala159=
NM_001122757.2:c.555T>G NP_001116229.1:p.Ala185=
NM_000306.4:c.477T>G MANE Select NP_000297.1:p.Ala159=
NM_001122757.3:c.555T>G NP_001116229.1:p.Ala185=