Canonical Allele Identifier: CA23067063
Gene: PLPP3 HGNC NCBI

Linked Data

dbSNP Id: rs144397500
gnomAD v2: 1-56966414-C-T
gnomAD v3: 1-56500742-C-T
gnomAD v4: 1-56500742-C-T
MyVariant Identifiers: chr1:g.56966414C>T (hg19) chr1:g.56500742C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500742C>T , CM000663.2:g.56500742C>T GRCh38
NC_000001.10:g.56966414C>T , CM000663.1:g.56966414C>T GRCh37
NC_000001.9:g.56739002C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4066G>A MANE Select ENSP00000360296.3:n.811-4066G>A
ENST00000641109.1:c.220-4066G>A ENSP00000493138.1:n.220-4066G>A
ENST00000641494.1:c.65-4066G>A
ENST00000642129.1:c.455-4066G>A
ENST00000371250.3:c.811-4066G>A ENSP00000360296.3:n.811-4066G>A
ENST00000459962.1:n.1797-4066G>A
ENST00000472957.1:n.296-4066G>A
NM_003713.4:c.811-4066G>A NP_003704.3:n.811-4066G>A
NM_003713.5:c.811-4066G>A MANE Select NP_003704.3:n.811-4066G>A
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