Canonical Allele Identifier: CA1381563889
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259855_87259864delinsTGAAACGGGA , CM000665.2:g.87259855_87259864delinsTGAAACGGGA GRCh38
NC_000003.11:g.87309005_87309014delinsTGAAACGGGA , CM000665.1:g.87309005_87309014delinsTGAAACGGGA GRCh37
NC_000003.10:g.87391695_87391704delinsTGAAACGGGA NCBI36
NG_008225.2:g.21724_21733delinsTCCCGTTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*30_*39delinsTCCCGTTTCA ENSP00000342931.3:n.*30_*39delinsTCCCGTTTCA
ENST00000350375.7:c.*30_*39delinsTCCCGTTTCA MANE Select ENSP00000263781.2:n.*30_*39delinsTCCCGTTTCA
ENST00000344265.7:c.*30_*39delinsTCCCGTTTCA ENSP00000342931.3:n.*30_*39delinsTCCCGTTTCA
ENST00000350375.6:c.*30_*39delinsTCCCGTTTCA ENSP00000263781.2:n.*30_*39delinsTCCCGTTTCA
NM_000306.3:c.*30_*39delinsTCCCGTTTCA NP_000297.1:n.*30_*39delinsTCCCGTTTCA
NM_001122757.2:c.*30_*39delinsTCCCGTTTCA NP_001116229.1:n.*30_*39delinsTCCCGTTTCA
NM_000306.4:c.*30_*39delinsTCCCGTTTCA MANE Select NP_000297.1:n.*30_*39delinsTCCCGTTTCA
NM_001122757.3:c.*30_*39delinsTCCCGTTTCA NP_001116229.1:n.*30_*39delinsTCCCGTTTCA