Canonical Allele Identifier: CA1381566353
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261918T= , CM000665.2:g.87261918T= GRCh38
NC_000003.11:g.87311068T= , CM000665.1:g.87311068T= GRCh37
NC_000003.10:g.87393758T= NCBI36
NG_008225.2:g.19670A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.682+153A= ENSP00000342931.3:n.682+153A=
ENST00000350375.7:c.604+153A= MANE Select ENSP00000263781.2:n.604+153A=
ENST00000344265.7:c.682+153A= ENSP00000342931.3:n.682+153A=
ENST00000350375.6:c.604+153A= ENSP00000263781.2:n.604+153A=
ENST00000560656.1:c.440-1814A= ENSP00000452610.1:n.440-1814A=
ENST00000561167.5:c.379+153A= ENSP00000454072.1:n.379+153A=
NM_000306.3:c.604+153A= NP_000297.1:n.604+153A=
NM_001122757.2:c.682+153A= NP_001116229.1:n.682+153A=
NM_000306.4:c.604+153A= MANE Select NP_000297.1:n.604+153A=
NM_001122757.3:c.682+153A= NP_001116229.1:n.682+153A=