Canonical Allele Identifier: CA434575705
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87311291G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262141G>C , CM000665.2:g.87262141G>C GRCh38
NC_000003.11:g.87311291G>C , CM000665.1:g.87311291G>C GRCh37
NC_000003.10:g.87393981G>C NCBI36
NG_008225.2:g.19447C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.612C>G ENSP00000342931.3:p.Leu204=
ENST00000350375.7:c.534C>G MANE Select ENSP00000263781.2:p.Leu178=
ENST00000344265.7:c.612C>G ENSP00000342931.3:p.Leu204=
ENST00000350375.6:c.534C>G ENSP00000263781.2:p.Leu178=
ENST00000560656.1:c.440-2037C>G ENSP00000452610.1:n.440-2037C>G
ENST00000561167.5:c.309C>G ENSP00000454072.1:p.Leu103=
NM_000306.3:c.534C>G NP_000297.1:p.Leu178=
NM_001122757.2:c.612C>G NP_001116229.1:p.Leu204=
NM_000306.4:c.534C>G MANE Select NP_000297.1:p.Leu178=
NM_001122757.3:c.612C>G NP_001116229.1:p.Leu204=