Canonical Allele Identifier: CA596482974

Gene: PLPP4

Linked Data

• dbSNP Id: rs1342382859
• gnomAD v2: 10-122279587-G-A
• gnomAD v3: 10-120520075-G-A
• gnomAD v4: 10-120520075-G-A
• MyVariant Identifiers: chr10:g.122279587G>A (hg19) ; chr10:g.120520075G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.120520075G>A , CM000672.2:g.120520075G>A	GRCh38
NC_000010.10:g.122279587G>A , CM000672.1:g.122279587G>A	GRCh37
NC_000010.9:g.122269577G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398250.6:c.321-896G>A MANE Select	ENSP00000381302.1:n.321-896G>A
ENST00000369073.3:c.291-896G>A	ENSP00000358069.3:n.291-896G>A
ENST00000398250.5:c.321-896G>A	ENSP00000381302.1:n.321-896G>A
ENST00000427079.5:c.321-896G>A	ENSP00000407979.1:n.321-896G>A
NM_001030059.1:c.321-896G>A	NP_001025230.1:n.321-896G>A
XM_005269592.1:c.321-896G>A	XP_005269649.1:n.321-896G>A
XM_006717685.2:c.282-896G>A	XP_006717748.1:n.282-896G>A
XM_006717686.2:c.321-896G>A	XP_006717749.1:n.321-896G>A
XM_006717688.2:c.-100-580G>A	XP_006717751.1:n.-100-580G>A
XM_011539444.1:c.315-896G>A	XP_011537746.1:n.315-896G>A
XM_011539445.1:c.321-896G>A	XP_011537747.1:n.321-896G>A
XM_011539446.1:c.256+6074G>A	XP_011537748.1:n.256+6074G>A
XM_011539447.1:c.-135-580G>A	XP_011537749.1:n.-135-580G>A
XM_011539448.1:c.-8-931G>A	XP_011537750.1:n.-8-931G>A
NM_001030059.2:c.321-896G>A	NP_001025230.1:n.321-896G>A
NM_001318166.1:c.320+1179G>A	NP_001305095.1:n.320+1179G>A
NM_001318167.1:c.256+6074G>A	NP_001305096.1:n.256+6074G>A
NM_001318168.1:c.165+16149G>A	NP_001305097.1:n.165+16149G>A
NM_001318169.1:c.165+16149G>A	NP_001305098.1:n.165+16149G>A
NR_134516.1:n.309+16149G>A
XM_005269592.2:c.321-896G>A	XP_005269649.1:n.321-896G>A
XM_006717685.4:c.282-896G>A	XP_006717748.1:n.282-896G>A
XM_006717686.4:c.321-896G>A	XP_006717749.1:n.321-896G>A
XM_011539444.3:c.315-896G>A	XP_011537746.1:n.315-896G>A
XM_011539445.2:c.321-896G>A	XP_011537747.1:n.321-896G>A
XM_017015820.1:c.282-896G>A	XP_016871309.1:n.282-896G>A
XM_017015823.1:c.165+16149G>A	XP_016871312.1:n.165+16149G>A
XM_017015824.2:c.165+16149G>A	XP_016871313.1:n.165+16149G>A
XM_024447860.1:c.-43-896G>A	XP_024303628.1:n.-43-896G>A
XM_024447861.1:c.-8-931G>A	XP_024303629.1:n.-8-931G>A
XM_024447862.1:c.-8-931G>A	XP_024303630.1:n.-8-931G>A
NM_001030059.3:c.321-896G>A MANE Select	NP_001025230.1:n.321-896G>A
NM_001318166.2:c.320+1179G>A	NP_001305095.1:n.320+1179G>A
NM_001318167.2:c.256+6074G>A	NP_001305096.1:n.256+6074G>A
NM_001318168.2:c.165+16149G>A	NP_001305097.1:n.165+16149G>A
NM_001318169.2:c.165+16149G>A	NP_001305098.1:n.165+16149G>A