Canonical Allele Identifier: CA1168598902

Gene: PLPP3

Linked Data

• dbSNP Id: rs1569860937

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.56500779T>G , CM000663.2:g.56500779T>G	GRCh38
NC_000001.10:g.56966451T>G , CM000663.1:g.56966451T>G	GRCh37
NC_000001.9:g.56739039T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371250.4:c.811-4103A>C MANE Select	ENSP00000360296.3:n.811-4103A>C
ENST00000641109.1:c.220-4103A>C	ENSP00000493138.1:n.220-4103A>C
ENST00000641494.1:c.65-4103A>C
ENST00000642129.1:c.455-4103A>C
ENST00000371250.3:c.811-4103A>C	ENSP00000360296.3:n.811-4103A>C
ENST00000459962.1:n.1797-4103A>C
ENST00000472957.1:n.296-4103A>C
NM_003713.4:c.811-4103A>C	NP_003704.3:n.811-4103A>C
NM_003713.5:c.811-4103A>C MANE Select	NP_003704.3:n.811-4103A>C