Canonical Allele Identifier: CA1168598935
Gene: PLPP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500815G= , CM000663.2:g.56500815G= GRCh38
NC_000001.10:g.56966487G= , CM000663.1:g.56966487G= GRCh37
NC_000001.9:g.56739075G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4139C= MANE Select ENSP00000360296.3:n.811-4139C=
ENST00000641109.1:c.220-4139C= ENSP00000493138.1:n.220-4139C=
ENST00000641494.1:c.65-4139C=
ENST00000642129.1:c.455-4139C=
ENST00000371250.3:c.811-4139C= ENSP00000360296.3:n.811-4139C=
ENST00000459962.1:n.1797-4139C=
ENST00000472957.1:n.296-4139C=
NM_003713.4:c.811-4139C= NP_003704.3:n.811-4139C=
NM_003713.5:c.811-4139C= MANE Select NP_003704.3:n.811-4139C=
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