Canonical Allele Identifier: CA596482966

Gene: PLPP4

Linked Data

• dbSNP Id: rs1362477706
• gnomAD v2: 10-122279421-C-T
• gnomAD v3: 10-120519909-C-T
• gnomAD v4: 10-120519909-C-T
• MyVariant Identifiers: chr10:g.122279421C>T (hg19) ; chr10:g.120519909C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.120519909C>T , CM000672.2:g.120519909C>T	GRCh38
NC_000010.10:g.122279421C>T , CM000672.1:g.122279421C>T	GRCh37
NC_000010.9:g.122269411C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398250.6:c.320+1013C>T MANE Select	ENSP00000381302.1:n.320+1013C>T
ENST00000369073.3:c.290+1013C>T	ENSP00000358069.3:n.290+1013C>T
ENST00000398250.5:c.320+1013C>T	ENSP00000381302.1:n.320+1013C>T
ENST00000427079.5:c.320+1013C>T	ENSP00000407979.1:n.320+1013C>T
NM_001030059.1:c.320+1013C>T	NP_001025230.1:n.320+1013C>T
XM_005269592.1:c.320+1013C>T	XP_005269649.1:n.320+1013C>T
XM_006717685.2:c.281+1013C>T	XP_006717748.1:n.281+1013C>T
XM_006717686.2:c.320+1013C>T	XP_006717749.1:n.320+1013C>T
XM_006717688.2:c.-100-746C>T	XP_006717751.1:n.-100-746C>T
XM_011539444.1:c.314+1013C>T	XP_011537746.1:n.314+1013C>T
XM_011539445.1:c.320+1013C>T	XP_011537747.1:n.320+1013C>T
XM_011539446.1:c.256+5908C>T	XP_011537748.1:n.256+5908C>T
XM_011539447.1:c.-135-746C>T	XP_011537749.1:n.-135-746C>T
XM_011539448.1:c.-9+1013C>T	XP_011537750.1:n.-9+1013C>T
NM_001030059.2:c.320+1013C>T	NP_001025230.1:n.320+1013C>T
NM_001318166.1:c.320+1013C>T	NP_001305095.1:n.320+1013C>T
NM_001318167.1:c.256+5908C>T	NP_001305096.1:n.256+5908C>T
NM_001318168.1:c.165+15983C>T	NP_001305097.1:n.165+15983C>T
NM_001318169.1:c.165+15983C>T	NP_001305098.1:n.165+15983C>T
NR_134516.1:n.309+15983C>T
XM_005269592.2:c.320+1013C>T	XP_005269649.1:n.320+1013C>T
XM_006717685.4:c.281+1013C>T	XP_006717748.1:n.281+1013C>T
XM_006717686.4:c.320+1013C>T	XP_006717749.1:n.320+1013C>T
XM_011539444.3:c.314+1013C>T	XP_011537746.1:n.314+1013C>T
XM_011539445.2:c.320+1013C>T	XP_011537747.1:n.320+1013C>T
XM_017015820.1:c.281+1013C>T	XP_016871309.1:n.281+1013C>T
XM_017015823.1:c.165+15983C>T	XP_016871312.1:n.165+15983C>T
XM_017015824.2:c.165+15983C>T	XP_016871313.1:n.165+15983C>T
XM_024447860.1:c.-44+1013C>T	XP_024303628.1:n.-44+1013C>T
XM_024447861.1:c.-9+1013C>T	XP_024303629.1:n.-9+1013C>T
XM_024447862.1:c.-9+1013C>T	XP_024303630.1:n.-9+1013C>T
NM_001030059.3:c.320+1013C>T MANE Select	NP_001025230.1:n.320+1013C>T
NM_001318166.2:c.320+1013C>T	NP_001305095.1:n.320+1013C>T
NM_001318167.2:c.256+5908C>T	NP_001305096.1:n.256+5908C>T
NM_001318168.2:c.165+15983C>T	NP_001305097.1:n.165+15983C>T
NM_001318169.2:c.165+15983C>T	NP_001305098.1:n.165+15983C>T