Canonical Allele Identifier: CA434579348

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309107C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259957C>G , CM000665.2:g.87259957C>G	GRCh38
NC_000003.11:g.87309107C>G , CM000665.1:g.87309107C>G	GRCh37
NC_000003.10:g.87391797C>G	NCBI36
NG_008225.2:g.21631G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.891G>C	ENSP00000342931.3:p.Arg297=
ENST00000350375.7:c.813G>C MANE Select	ENSP00000263781.2:p.Arg271=
ENST00000344265.7:c.891G>C	ENSP00000342931.3:p.Arg297=
ENST00000350375.6:c.813G>C	ENSP00000263781.2:p.Arg271=
ENST00000560656.1:c.587G>C	ENSP00000452610.1:n.587G>C
ENST00000561167.5:c.588G>C	ENSP00000454072.1:p.Arg196=
NM_000306.3:c.813G>C	NP_000297.1:p.Arg271=
NM_001122757.2:c.891G>C	NP_001116229.1:p.Arg297=
NM_000306.4:c.813G>C MANE Select	NP_000297.1:p.Arg271=
NM_001122757.3:c.891G>C	NP_001116229.1:p.Arg297=