Canonical Allele Identifier: CA1168598843
Gene: PLPP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500715A= , CM000663.2:g.56500715A= GRCh38
NC_000001.10:g.56966387A= , CM000663.1:g.56966387A= GRCh37
NC_000001.9:g.56738975A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4039T= MANE Select ENSP00000360296.3:n.811-4039T=
ENST00000641109.1:c.220-4039T= ENSP00000493138.1:n.220-4039T=
ENST00000641494.1:c.65-4039T=
ENST00000642129.1:c.455-4039T=
ENST00000371250.3:c.811-4039T= ENSP00000360296.3:n.811-4039T=
ENST00000459962.1:n.1797-4039T=
ENST00000472957.1:n.296-4039T=
NM_003713.4:c.811-4039T= NP_003704.3:n.811-4039T=
NM_003713.5:c.811-4039T= MANE Select NP_003704.3:n.811-4039T=