Canonical Allele Identifier: CA2501137
Community Standard Title: NM_000306.4(POU1F1):c.605-18_605-15dup
Gene: POU1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261351_87261354dup , CM000665.2:g.87261351_87261354dup GRCh38
NC_000003.11:g.87310501_87310504dup , CM000665.1:g.87310501_87310504dup GRCh37
NC_000003.10:g.87393191_87393194dup NCBI36
NG_008225.2:g.20237_20240dup

Transcript Alleles

HGVS Amino-acid Change
NM_000306.4:c.605-18_605-15dup MANE Select NP_000297.1:n.605-18_605-15dup
ENST00000350375.7:c.605-18_605-15dup MANE Select ENSP00000263781.2:n.605-18_605-15dup
NM_000306.3:c.605-18_605-15dup NP_000297.1:n.605-18_605-15dup
NM_001122757.2:c.683-18_683-15dup NP_001116229.1:n.683-18_683-15dup
NM_001122757.3:c.683-18_683-15dup NP_001116229.1:n.683-18_683-15dup
ENST00000344265.7:c.683-18_683-15dup ENSP00000342931.3:n.683-18_683-15dup
ENST00000344265.8:c.683-18_683-15dup ENSP00000342931.3:n.683-18_683-15dup
ENST00000350375.6:c.605-18_605-15dup ENSP00000263781.2:n.605-18_605-15dup
ENST00000560656.1:c.440-1247_440-1244dup ENSP00000452610.1:n.440-1247_440-1244dup
ENST00000561167.5:c.380-18_380-15dup ENSP00000454072.1:n.380-18_380-15dup