Canonical Allele Identifier: CA434575755
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87311366A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262216A>G , CM000665.2:g.87262216A>G GRCh38
NC_000003.11:g.87311366A>G , CM000665.1:g.87311366A>G GRCh37
NC_000003.10:g.87394056A>G NCBI36
NG_008225.2:g.19372T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.537T>C ENSP00000342931.3:p.Val179=
ENST00000350375.7:c.459T>C MANE Select ENSP00000263781.2:p.Val153=
ENST00000344265.7:c.537T>C ENSP00000342931.3:p.Val179=
ENST00000350375.6:c.459T>C ENSP00000263781.2:p.Val153=
ENST00000560656.1:c.439+2072T>C ENSP00000452610.1:n.439+2072T>C
ENST00000561167.5:c.234T>C ENSP00000454072.1:p.Val78=
NM_000306.3:c.459T>C NP_000297.1:p.Val153=
NM_001122757.2:c.537T>C NP_001116229.1:p.Val179=
NM_000306.4:c.459T>C MANE Select NP_000297.1:p.Val153=
NM_001122757.3:c.537T>C NP_001116229.1:p.Val179=