Canonical Allele Identifier: CA1381534922
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264253A= , CM000665.2:g.87264253A= GRCh38
NC_000003.11:g.87313403A= , CM000665.1:g.87313403A= GRCh37
NC_000003.10:g.87396093A= NCBI36
NG_008225.2:g.17335T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.517+35T= ENSP00000342931.3:n.517+35T=
ENST00000350375.7:c.439+35T= MANE Select ENSP00000263781.2:n.439+35T=
ENST00000344265.7:c.517+35T= ENSP00000342931.3:n.517+35T=
ENST00000350375.6:c.439+35T= ENSP00000263781.2:n.439+35T=
ENST00000560656.1:c.439+35T= ENSP00000452610.1:n.439+35T=
ENST00000561167.5:c.215-2018T= ENSP00000454072.1:n.215-2018T=
NM_000306.3:c.439+35T= NP_000297.1:n.439+35T=
NM_001122757.2:c.517+35T= NP_001116229.1:n.517+35T=
NM_000306.4:c.439+35T= MANE Select NP_000297.1:n.439+35T=
NM_001122757.3:c.517+35T= NP_001116229.1:n.517+35T=