Canonical Allele Identifier: CA353692757
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1199287134
gnomAD v2: 3-87311250-T-C
gnomAD v4: 3-87262100-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262100T>C , CM000665.2:g.87262100T>C GRCh38
NC_000003.11:g.87311250T>C , CM000665.1:g.87311250T>C GRCh37
NC_000003.10:g.87393940T>C NCBI36
NG_008225.2:g.19488A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.653A>G ENSP00000342931.3:p.Lys218Arg
ENST00000350375.7:c.575A>G MANE Select ENSP00000263781.2:p.Lys192Arg
ENST00000344265.7:c.653A>G ENSP00000342931.3:p.Lys218Arg
ENST00000350375.6:c.575A>G ENSP00000263781.2:p.Lys192Arg
ENST00000560656.1:c.440-1996A>G ENSP00000452610.1:n.440-1996A>G
ENST00000561167.5:c.350A>G ENSP00000454072.1:p.Lys117Arg
NM_000306.3:c.575A>G NP_000297.1:p.Lys192Arg
NM_001122757.2:c.653A>G NP_001116229.1:p.Lys218Arg
NM_000306.4:c.575A>G MANE Select NP_000297.1:p.Lys192Arg
NM_001122757.3:c.653A>G NP_001116229.1:p.Lys218Arg