Canonical Allele Identifier: CA737145123
Gene: PLPP3 HGNC NCBI

Linked Data

dbSNP Id: rs1169598726
MyVariant Identifiers: chr1:g.56966321G>T (hg19) chr1:g.56500649G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500649G>T , CM000663.2:g.56500649G>T GRCh38
NC_000001.10:g.56966321G>T , CM000663.1:g.56966321G>T GRCh37
NC_000001.9:g.56738909G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-3973C>A MANE Select ENSP00000360296.3:n.811-3973C>A
ENST00000641109.1:c.220-3973C>A ENSP00000493138.1:n.220-3973C>A
ENST00000641494.1:c.65-3973C>A
ENST00000642129.1:c.455-3973C>A
ENST00000371250.3:c.811-3973C>A ENSP00000360296.3:n.811-3973C>A
ENST00000459962.1:n.1797-3973C>A
ENST00000472957.1:n.296-3973C>A
NM_003713.4:c.811-3973C>A NP_003704.3:n.811-3973C>A
NM_003713.5:c.811-3973C>A MANE Select NP_003704.3:n.811-3973C>A
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