Canonical Allele Identifier: CA434575749

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87311357G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262207G>C , CM000665.2:g.87262207G>C	GRCh38
NC_000003.11:g.87311357G>C , CM000665.1:g.87311357G>C	GRCh37
NC_000003.10:g.87394047G>C	NCBI36
NG_008225.2:g.19381C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.546C>G	ENSP00000342931.3:p.Ala182=
ENST00000350375.7:c.468C>G MANE Select	ENSP00000263781.2:p.Ala156=
ENST00000344265.7:c.546C>G	ENSP00000342931.3:p.Ala182=
ENST00000350375.6:c.468C>G	ENSP00000263781.2:p.Ala156=
ENST00000560656.1:c.439+2081C>G	ENSP00000452610.1:n.439+2081C>G
ENST00000561167.5:c.243C>G	ENSP00000454072.1:p.Ala81=
NM_000306.3:c.468C>G	NP_000297.1:p.Ala156=
NM_001122757.2:c.546C>G	NP_001116229.1:p.Ala182=
NM_000306.4:c.468C>G MANE Select	NP_000297.1:p.Ala156=
NM_001122757.3:c.546C>G	NP_001116229.1:p.Ala182=