Canonical Allele Identifier: CA2739275168
Gene: POU4F3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2869928
ClinVar RCV Id: RCV003700931

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339841_146339845del , CM000667.2:g.146339841_146339845del GRCh38
NC_000005.9:g.145719404_145719408del , CM000667.1:g.145719404_145719408del GRCh37
NC_000005.8:g.145699597_145699601del NCBI36
NG_011885.1:g.5818_5822del

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.414_418del MANE Select ENSP00000495718.1:p.Val139AlafsTer?
ENST00000230732.4:c.414_418del ENSP00000230732.4:p.Val139AlafsTer?
NM_002700.2:c.414_418del NP_002691.1:p.Val139AlafsTer?
NM_002700.3:c.414_418del MANE Select NP_002691.1:p.Val139AlafsTer?