Canonical Allele Identifier: CA1168598871
Gene: PLPP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500739_56500752delinsTCACGCCTAAAATC , CM000663.2:g.56500739_56500752delinsTCACGCCTAAAATC GRCh38
NC_000001.10:g.56966411_56966424delinsTCACGCCTAAAATC , CM000663.1:g.56966411_56966424delinsTCACGCCTAAAATC GRCh37
NC_000001.9:g.56738999_56739012delinsTCACGCCTAAAATC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4076_811-4063delinsGATTTTAGGCGTGA MANE Select ENSP00000360296.3:n.811-4076_811-4063delinsGATTTTAGGCGTGA
ENST00000641109.1:c.220-4076_220-4063delinsGATTTTAGGCGTGA ENSP00000493138.1:n.220-4076_220-4063delinsGATTTTAGGCGTGA
ENST00000641494.1:c.65-4076_65-4063delinsGATTTTAGGCGTGA
ENST00000642129.1:c.455-4076_455-4063delinsGATTTTAGGCGTGA
ENST00000371250.3:c.811-4076_811-4063delinsGATTTTAGGCGTGA ENSP00000360296.3:n.811-4076_811-4063delinsGATTTTAGGCGTGA
ENST00000459962.1:n.1797-4076_1797-4063delinsGATTTTAGGCGTGA
ENST00000472957.1:n.296-4076_296-4063delinsGATTTTAGGCGTGA
NM_003713.4:c.811-4076_811-4063delinsGATTTTAGGCGTGA NP_003704.3:n.811-4076_811-4063delinsGATTTTAGGCGTGA
NM_003713.5:c.811-4076_811-4063delinsGATTTTAGGCGTGA MANE Select NP_003704.3:n.811-4076_811-4063delinsGATTTTAGGCGTGA