Canonical Allele Identifier: CA524845602

Gene: PLPPR5

Linked Data

• dbSNP Id: rs1408384396
• gnomAD v2: 1-99453392-ATT-A
• gnomAD v3: 1-98987836-ATT-A
• gnomAD v4: 1-98987836-ATT-A
• MyVariant Identifiers: chr1:g.99453393_99453394del (hg19) ; chr1:g.98987837_98987838del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.98987838_98987839del , CM000663.2:g.98987838_98987839del	GRCh38
NC_000001.10:g.99453394_99453395del , CM000663.1:g.99453394_99453395del	GRCh37
NC_000001.9:g.99225982_99225983del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696571.1:c.73-31097_73-31096del	ENSP00000512726.1:n.73-31097_73-31096del
ENST00000263177.5:c.237+16597_237+16598del MANE Select	ENSP00000263177.4:n.237+16597_237+16598del
ENST00000672681.1:c.237+16597_237+16598del	ENSP00000500930.1:n.237+16597_237+16598del
ENST00000263177.4:c.237+16597_237+16598del	ENSP00000263177.4:n.237+16597_237+16598del
ENST00000370188.7:c.237+16597_237+16598del	ENSP00000359207.3:n.237+16597_237+16598del
NM_001010861.2:c.237+16597_237+16598del	NP_001010861.1:n.237+16597_237+16598del
NM_001037317.1:c.237+16597_237+16598del	NP_001032394.1:n.237+16597_237+16598del
XM_011540836.1:c.237+16597_237+16598del	XP_011539138.1:n.237+16597_237+16598del
XM_011540837.1:c.237+16597_237+16598del	XP_011539139.1:n.237+16597_237+16598del
XM_011540838.1:c.189+16597_189+16598del	XP_011539140.1:n.189+16597_189+16598del
XM_011540839.1:c.189+16597_189+16598del	XP_011539141.1:n.189+16597_189+16598del
XM_011540836.2:c.237+16597_237+16598del	XP_011539138.1:n.237+16597_237+16598del
XM_011540838.3:c.189+16597_189+16598del	XP_011539140.1:n.189+16597_189+16598del
NM_001037317.2:c.237+16597_237+16598del MANE Select	NP_001032394.1:n.237+16597_237+16598del
NM_001010861.3:c.237+16597_237+16598del	NP_001010861.1:n.237+16597_237+16598del