Canonical Allele Identifier: CA79036903
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs928420971
gnomAD v2: 3-87313491-A-T
gnomAD v3: 3-87264341-A-T
gnomAD v4: 3-87264341-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264341A>T , CM000665.2:g.87264341A>T GRCh38
NC_000003.11:g.87313491A>T , CM000665.1:g.87313491A>T GRCh37
NC_000003.10:g.87396181A>T NCBI36
NG_008225.2:g.17247T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.464T>A ENSP00000342931.3:p.Ile155Asn
ENST00000350375.7:c.386T>A MANE Select ENSP00000263781.2:p.Ile129Asn
ENST00000344265.7:c.464T>A ENSP00000342931.3:p.Ile155Asn
ENST00000350375.6:c.386T>A ENSP00000263781.2:p.Ile129Asn
ENST00000560656.1:c.386T>A ENSP00000452610.1:p.Ile129Asn
ENST00000561167.5:c.215-2106T>A ENSP00000454072.1:n.215-2106T>A
NM_000306.3:c.386T>A NP_000297.1:p.Ile129Asn
NM_001122757.2:c.464T>A NP_001116229.1:p.Ile155Asn
NM_000306.4:c.386T>A MANE Select NP_000297.1:p.Ile129Asn
NM_001122757.3:c.464T>A NP_001116229.1:p.Ile155Asn