Canonical Allele Identifier: CA1168598802
Gene: PLPP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500625A= , CM000663.2:g.56500625A= GRCh38
NC_000001.10:g.56966297A= , CM000663.1:g.56966297A= GRCh37
NC_000001.9:g.56738885A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371250.4:c.811-3949T= MANE Select ENSP00000360296.3:n.811-3949T=
ENST00000641109.1:c.220-3949T= ENSP00000493138.1:n.220-3949T=
ENST00000641494.1:c.65-3949T=
ENST00000642129.1:c.455-3949T=
ENST00000371250.3:c.811-3949T= ENSP00000360296.3:n.811-3949T=
ENST00000459962.1:n.1797-3949T=
ENST00000472957.1:n.296-3949T=
NM_003713.4:c.811-3949T= NP_003704.3:n.811-3949T=
NM_003713.5:c.811-3949T= MANE Select NP_003704.3:n.811-3949T=