Canonical Allele Identifier: CA434579083
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87309044T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259894T>C , CM000665.2:g.87259894T>C GRCh38
NC_000003.11:g.87309044T>C , CM000665.1:g.87309044T>C GRCh37
NC_000003.10:g.87391734T>C NCBI36
NG_008225.2:g.21694A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.954A>G ENSP00000342931.3:p.Ter318=
ENST00000350375.7:c.876A>G MANE Select ENSP00000263781.2:p.Ter292=
ENST00000344265.7:c.954A>G ENSP00000342931.3:p.Ter318=
ENST00000350375.6:c.876A>G ENSP00000263781.2:p.Ter292=
NM_000306.3:c.876A>G NP_000297.1:p.Ter292=
NM_001122757.2:c.954A>G NP_001116229.1:p.Ter318=
NM_000306.4:c.876A>G MANE Select NP_000297.1:p.Ter292=
NM_001122757.3:c.954A>G NP_001116229.1:p.Ter318=