Canonical Allele Identifier: CA353698265
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87260037T>G , CM000665.2:g.87260037T>G GRCh38
NC_000003.11:g.87309187T>G , CM000665.1:g.87309187T>G GRCh37
NC_000003.10:g.87391877T>G NCBI36
NG_008225.2:g.21551A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.811A>C ENSP00000342931.3:p.Met271Leu
ENST00000350375.7:c.733A>C MANE Select ENSP00000263781.2:p.Met245Leu
ENST00000344265.7:c.811A>C ENSP00000342931.3:p.Met271Leu
ENST00000350375.6:c.733A>C ENSP00000263781.2:p.Met245Leu
ENST00000560656.1:c.507A>C ENSP00000452610.1:p.Ser169=
ENST00000561167.5:c.508A>C ENSP00000454072.1:p.Met170Leu
NM_000306.3:c.733A>C NP_000297.1:p.Met245Leu
NM_001122757.2:c.811A>C NP_001116229.1:p.Met271Leu
NM_000306.4:c.733A>C MANE Select NP_000297.1:p.Met245Leu
NM_001122757.3:c.811A>C NP_001116229.1:p.Met271Leu