Canonical Allele Identifier: CA911577600

Gene: POU1F1

Linked Data

• dbSNP Id: rs1218532879
• MyVariant Identifiers: chr3:g.87311055T>A (hg19) ; chr3:g.87261905T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87261905T>A , CM000665.2:g.87261905T>A	GRCh38
NC_000003.11:g.87311055T>A , CM000665.1:g.87311055T>A	GRCh37
NC_000003.10:g.87393745T>A	NCBI36
NG_008225.2:g.19683A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.682+166A>T	ENSP00000342931.3:n.682+166A>T
ENST00000350375.7:c.604+166A>T MANE Select	ENSP00000263781.2:n.604+166A>T
ENST00000344265.7:c.682+166A>T	ENSP00000342931.3:n.682+166A>T
ENST00000350375.6:c.604+166A>T	ENSP00000263781.2:n.604+166A>T
ENST00000560656.1:c.440-1801A>T	ENSP00000452610.1:n.440-1801A>T
ENST00000561167.5:c.379+166A>T	ENSP00000454072.1:n.379+166A>T
NM_000306.3:c.604+166A>T	NP_000297.1:n.604+166A>T
NM_001122757.2:c.682+166A>T	NP_001116229.1:n.682+166A>T
NM_000306.4:c.604+166A>T MANE Select	NP_000297.1:n.604+166A>T
NM_001122757.3:c.682+166A>T	NP_001116229.1:n.682+166A>T