Canonical Allele Identifier: CA79036429

Gene: POU1F1

Linked Data

• dbSNP Id: rs369739158
• gnomAD v3: 3-87259746-CTT-C
• gnomAD v4: 3-87259746-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259753_87259754del , CM000665.2:g.87259753_87259754del	GRCh38
NC_000003.11:g.87308903_87308904del , CM000665.1:g.87308903_87308904del	GRCh37
NC_000003.10:g.87391593_87391594del	NCBI36
NG_008225.2:g.21840_21841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.*146_*147del	ENSP00000342931.3:n.*146_*147del
ENST00000350375.7:c.*146_*147del MANE Select	ENSP00000263781.2:n.*146_*147del
ENST00000344265.7:c.*146_*147del	ENSP00000342931.3:n.*146_*147del
ENST00000350375.6:c.*146_*147del	ENSP00000263781.2:n.*146_*147del
NM_000306.3:c.*146_*147del	NP_000297.1:n.*146_*147del
NM_001122757.2:c.*146_*147del	NP_001116229.1:n.*146_*147del
NM_000306.4:c.*146_*147del MANE Select	NP_000297.1:n.*146_*147del
NM_001122757.3:c.*146_*147del	NP_001116229.1:n.*146_*147del