Canonical Allele Identifier: CA1168598934
Gene: PLPP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500813T= , CM000663.2:g.56500813T= GRCh38
NC_000001.10:g.56966485T= , CM000663.1:g.56966485T= GRCh37
NC_000001.9:g.56739073T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4137A= MANE Select ENSP00000360296.3:n.811-4137A=
ENST00000641109.1:c.220-4137A= ENSP00000493138.1:n.220-4137A=
ENST00000641494.1:c.65-4137A=
ENST00000642129.1:c.455-4137A=
ENST00000371250.3:c.811-4137A= ENSP00000360296.3:n.811-4137A=
ENST00000459962.1:n.1797-4137A=
ENST00000472957.1:n.296-4137A=
NM_003713.4:c.811-4137A= NP_003704.3:n.811-4137A=
NM_003713.5:c.811-4137A= MANE Select NP_003704.3:n.811-4137A=
Search 100 bp 5'
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