Canonical Allele Identifier: CA353698112

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309120T>G (hg19) ; chr3:g.87259970T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259970T>G , CM000665.2:g.87259970T>G	GRCh38
NC_000003.11:g.87309120T>G , CM000665.1:g.87309120T>G	GRCh37
NC_000003.10:g.87391810T>G	NCBI36
NG_008225.2:g.21618A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.878A>C	ENSP00000342931.3:p.Gln293Pro
ENST00000350375.7:c.800A>C MANE Select	ENSP00000263781.2:p.Gln267Pro
ENST00000344265.7:c.878A>C	ENSP00000342931.3:p.Gln293Pro
ENST00000350375.6:c.800A>C	ENSP00000263781.2:p.Gln267Pro
ENST00000560656.1:c.574A>C	ENSP00000452610.1:n.574A>C
ENST00000561167.5:c.575A>C	ENSP00000454072.1:p.Gln192Pro
NM_000306.3:c.800A>C	NP_000297.1:p.Gln267Pro
NM_001122757.2:c.878A>C	NP_001116229.1:p.Gln293Pro
NM_000306.4:c.800A>C MANE Select	NP_000297.1:p.Gln267Pro
NM_001122757.3:c.878A>C	NP_001116229.1:p.Gln293Pro