Canonical Allele Identifier: CA353693125

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87311373G>C (hg19) ; chr3:g.87262223G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262223G>C , CM000665.2:g.87262223G>C	GRCh38
NC_000003.11:g.87311373G>C , CM000665.1:g.87311373G>C	GRCh37
NC_000003.10:g.87394063G>C	NCBI36
NG_008225.2:g.19365C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.530C>G	ENSP00000342931.3:p.Thr177Arg
ENST00000350375.7:c.452C>G MANE Select	ENSP00000263781.2:p.Thr151Arg
ENST00000344265.7:c.530C>G	ENSP00000342931.3:p.Thr177Arg
ENST00000350375.6:c.452C>G	ENSP00000263781.2:p.Thr151Arg
ENST00000560656.1:c.439+2065C>G	ENSP00000452610.1:n.439+2065C>G
ENST00000561167.5:c.227C>G	ENSP00000454072.1:p.Thr76Arg
NM_000306.3:c.452C>G	NP_000297.1:p.Thr151Arg
NM_001122757.2:c.530C>G	NP_001116229.1:p.Thr177Arg
NM_000306.4:c.452C>G MANE Select	NP_000297.1:p.Thr151Arg
NM_001122757.3:c.530C>G	NP_001116229.1:p.Thr177Arg