Canonical Allele Identifier: CA1381566373
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261928_87261929delinsTA , CM000665.2:g.87261928_87261929delinsTA GRCh38
NC_000003.11:g.87311078_87311079delinsTA , CM000665.1:g.87311078_87311079delinsTA GRCh37
NC_000003.10:g.87393768_87393769delinsTA NCBI36
NG_008225.2:g.19659_19660delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.682+142_682+143delinsTA ENSP00000342931.3:n.682+142_682+143delinsTA
ENST00000350375.7:c.604+142_604+143delinsTA MANE Select ENSP00000263781.2:n.604+142_604+143delinsTA
ENST00000344265.7:c.682+142_682+143delinsTA ENSP00000342931.3:n.682+142_682+143delinsTA
ENST00000350375.6:c.604+142_604+143delinsTA ENSP00000263781.2:n.604+142_604+143delinsTA
ENST00000560656.1:c.440-1825_440-1824delinsTA ENSP00000452610.1:n.440-1825_440-1824delinsTA
ENST00000561167.5:c.379+142_379+143delinsTA ENSP00000454072.1:n.379+142_379+143delinsTA
NM_000306.3:c.604+142_604+143delinsTA NP_000297.1:n.604+142_604+143delinsTA
NM_001122757.2:c.682+142_682+143delinsTA NP_001116229.1:n.682+142_682+143delinsTA
NM_000306.4:c.604+142_604+143delinsTA MANE Select NP_000297.1:n.604+142_604+143delinsTA
NM_001122757.3:c.682+142_682+143delinsTA NP_001116229.1:n.682+142_682+143delinsTA