Canonical Allele Identifier: CA1381564261
Gene: POU1F1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260123_87260124delinsAG , CM000665.2:g.87260123_87260124delinsAG GRCh38
NC_000003.11:g.87309273_87309274delinsAG , CM000665.1:g.87309273_87309274delinsAG GRCh37
NC_000003.10:g.87391963_87391964delinsAG NCBI36
NG_008225.2:g.21464_21465delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.744-20_744-19delinsCT ENSP00000342931.3:n.744-20_744-19delinsCT...
ENST00000350375.7:c.666-20_666-19delinsCT MANE Select ENSP00000263781.2:n.666-20_666-19delinsCT...
ENST00000344265.7:c.744-20_744-19delinsCT ENSP00000342931.3:n.744-20_744-19delinsCT...
ENST00000350375.6:c.666-20_666-19delinsCT ENSP00000263781.2:n.666-20_666-19delinsCT...
ENST00000560656.1:c.440-20_440-19delinsCT ENSP00000452610.1:n.440-20_440-19delinsCT...
ENST00000561167.5:c.441-20_441-19delinsCT ENSP00000454072.1:n.441-20_441-19delinsCT...
NM_000306.3:c.666-20_666-19delinsCT NP_000297.1:n.666-20_666-19delinsCT
NM_001122757.2:c.744-20_744-19delinsCT NP_001116229.1:n.744-20_744-19delinsCT
NM_000306.4:c.666-20_666-19delinsCT MANE Select NP_000297.1:n.666-20_666-19delinsCT
NM_001122757.3:c.744-20_744-19delinsCT NP_001116229.1:n.744-20_744-19delinsCT
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