Canonical Allele Identifier: CA23067062

Gene: PLPP3

Linked Data

• dbSNP Id: rs545388420
• gnomAD v2: 1-56966411-TCACG-T
• gnomAD v3: 1-56500739-TCACG-T
• gnomAD v4: 1-56500739-TCACG-T
• MyVariant Identifiers: chr1:g.56966412_56966415del (hg19) ; chr1:g.56500740_56500743del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.56500741_56500744del , CM000663.2:g.56500741_56500744del	GRCh38
NC_000001.10:g.56966413_56966416del , CM000663.1:g.56966413_56966416del	GRCh37
NC_000001.9:g.56739001_56739004del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371250.4:c.811-4067_811-4064del MANE Select	ENSP00000360296.3:n.811-4067_811-4064del
ENST00000641109.1:c.220-4067_220-4064del	ENSP00000493138.1:n.220-4067_220-4064del
ENST00000641494.1:c.65-4067_65-4064del
ENST00000642129.1:c.455-4067_455-4064del
ENST00000371250.3:c.811-4067_811-4064del	ENSP00000360296.3:n.811-4067_811-4064del
ENST00000459962.1:n.1797-4067_1797-4064del
ENST00000472957.1:n.296-4067_296-4064del
NM_003713.4:c.811-4067_811-4064del	NP_003704.3:n.811-4067_811-4064del
NM_003713.5:c.811-4067_811-4064del MANE Select	NP_003704.3:n.811-4067_811-4064del