Canonical Allele Identifier: CA1168598879
Gene: PLPP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500746_56500755delinsTAAAATCCCA , CM000663.2:g.56500746_56500755delinsTAAAATCCCA GRCh38
NC_000001.10:g.56966418_56966427delinsTAAAATCCCA , CM000663.1:g.56966418_56966427delinsTAAAATCCCA GRCh37
NC_000001.9:g.56739006_56739015delinsTAAAATCCCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4079_811-4070delinsTGGGATTTTA MANE Select ENSP00000360296.3:n.811-4079_811-4070delinsTGGGATTTTA
ENST00000641109.1:c.220-4079_220-4070delinsTGGGATTTTA ENSP00000493138.1:n.220-4079_220-4070delinsTGGGATTTTA
ENST00000641494.1:c.65-4079_65-4070delinsTGGGATTTTA
ENST00000642129.1:c.455-4079_455-4070delinsTGGGATTTTA
ENST00000371250.3:c.811-4079_811-4070delinsTGGGATTTTA ENSP00000360296.3:n.811-4079_811-4070delinsTGGGATTTTA
ENST00000459962.1:n.1797-4079_1797-4070delinsTGGGATTTTA
ENST00000472957.1:n.296-4079_296-4070delinsTGGGATTTTA
NM_003713.4:c.811-4079_811-4070delinsTGGGATTTTA NP_003704.3:n.811-4079_811-4070delinsTGGGATTTTA
NM_003713.5:c.811-4079_811-4070delinsTGGGATTTTA MANE Select NP_003704.3:n.811-4079_811-4070delinsTGGGATTTTA