Canonical Allele Identifier: CA1381534933
Gene: POU1F1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264267T= , CM000665.2:g.87264267T= GRCh38
NC_000003.11:g.87313417T= , CM000665.1:g.87313417T= GRCh37
NC_000003.10:g.87396107T= NCBI36
NG_008225.2:g.17321A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.517+21A= ENSP00000342931.3:n.517+21A=
ENST00000350375.7:c.439+21A= MANE Select ENSP00000263781.2:n.439+21A=
ENST00000344265.7:c.517+21A= ENSP00000342931.3:n.517+21A=
ENST00000350375.6:c.439+21A= ENSP00000263781.2:n.439+21A=
ENST00000560656.1:c.439+21A= ENSP00000452610.1:n.439+21A=
ENST00000561167.5:c.215-2032A= ENSP00000454072.1:n.215-2032A=
NM_000306.3:c.439+21A= NP_000297.1:n.439+21A=
NM_001122757.2:c.517+21A= NP_001116229.1:n.517+21A=
NM_000306.4:c.439+21A= MANE Select NP_000297.1:n.439+21A=
NM_001122757.3:c.517+21A= NP_001116229.1:n.517+21A=
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