Canonical Allele Identifier: CA353698250
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260032C>A , CM000665.2:g.87260032C>A GRCh38
NC_000003.11:g.87309182C>A , CM000665.1:g.87309182C>A GRCh37
NC_000003.10:g.87391872C>A NCBI36
NG_008225.2:g.21556G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.816G>T ENSP00000342931.3:p.Arg272Ser
ENST00000350375.7:c.738G>T MANE Select ENSP00000263781.2:p.Arg246Ser
ENST00000344265.7:c.816G>T ENSP00000342931.3:p.Arg272Ser
ENST00000350375.6:c.738G>T ENSP00000263781.2:p.Arg246Ser
ENST00000560656.1:c.512G>T ENSP00000452610.1:n.512G>T
ENST00000561167.5:c.513G>T ENSP00000454072.1:p.Arg171Ser
NM_000306.3:c.738G>T NP_000297.1:p.Arg246Ser
NM_001122757.2:c.816G>T NP_001116229.1:p.Arg272Ser
NM_000306.4:c.738G>T MANE Select NP_000297.1:p.Arg246Ser
NM_001122757.3:c.816G>T NP_001116229.1:p.Arg272Ser