Canonical Allele Identifier: CA911576020

Gene: POU1F1

Linked Data

• dbSNP Id: rs1489834298
• gnomAD v3: 3-87260120-CAT-C
• gnomAD v4: 3-87260120-CAT-C
• MyVariant Identifiers: chr3:g.87309271_87309272del (hg19) ; chr3:g.87260121_87260122del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87260122_87260123del , CM000665.2:g.87260122_87260123del	GRCh38
NC_000003.11:g.87309272_87309273del , CM000665.1:g.87309272_87309273del	GRCh37
NC_000003.10:g.87391962_87391963del	NCBI36
NG_008225.2:g.21466_21467del

Transcript Alleles

HGVS	Amino-acid change
ENST00000344265.8:c.744-18_744-17del	ENSP00000342931.3:n.744-18_744-17del
ENST00000350375.7:c.666-18_666-17del MANE Select	ENSP00000263781.2:n.666-18_666-17del
ENST00000344265.7:c.744-18_744-17del	ENSP00000342931.3:n.744-18_744-17del
ENST00000350375.6:c.666-18_666-17del	ENSP00000263781.2:n.666-18_666-17del
ENST00000560656.1:c.440-18_440-17del	ENSP00000452610.1:n.440-18_440-17del
ENST00000561167.5:c.441-18_441-17del	ENSP00000454072.1:n.441-18_441-17del
NM_000306.3:c.666-18_666-17del	NP_000297.1:n.666-18_666-17del
NM_001122757.2:c.744-18_744-17del	NP_001116229.1:n.744-18_744-17del
NM_000306.4:c.666-18_666-17del MANE Select	NP_000297.1:n.666-18_666-17del
NM_001122757.3:c.744-18_744-17del	NP_001116229.1:n.744-18_744-17del