Canonical Allele Identifier: CA2666629310
Gene: POU1F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259753_87259754insAA , CM000665.2:g.87259753_87259754insAA GRCh38
NC_000003.11:g.87308903_87308904insAA , CM000665.1:g.87308903_87308904insAA GRCh37
NC_000003.10:g.87391593_87391594insAA NCBI36
NG_008225.2:g.21834_21835insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*140_*141insTT ENSP00000342931.3:n.*140_*141insTT
ENST00000350375.7:c.*140_*141insTT MANE Select ENSP00000263781.2:n.*140_*141insTT
ENST00000344265.7:c.*140_*141insTT ENSP00000342931.3:n.*140_*141insTT
ENST00000350375.6:c.*140_*141insTT ENSP00000263781.2:n.*140_*141insTT
NM_000306.3:c.*140_*141insTT NP_000297.1:n.*140_*141insTT
NM_001122757.2:c.*140_*141insTT NP_001116229.1:n.*140_*141insTT
NM_000306.4:c.*140_*141insTT MANE Select NP_000297.1:n.*140_*141insTT
NM_001122757.3:c.*140_*141insTT NP_001116229.1:n.*140_*141insTT