Canonical Allele Identifier: CA930987015
Gene: LIPA HGNC NCBI

Linked Data

dbSNP Id: rs1842716520

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89222723del , CM000672.2:g.89222723del GRCh38
NC_000010.10:g.90982480del , CM000672.1:g.90982480del GRCh37
NC_000010.9:g.90972460del NCBI36
NG_008194.1:g.34181del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.823-141del MANE Select ENSP00000337354.5:n.823-141del
ENST00000336233.9:c.823-141del ENSP00000337354.5:n.823-141del
ENST00000371837.5:c.655-141del ENSP00000360903.1:n.655-141del
ENST00000428800.5:c.823-141del ENSP00000388415.1:n.823-141del
ENST00000456827.5:c.475-141del ENSP00000413019.2:n.475-141del
NM_000235.3:c.823-141del NP_000226.2:n.823-141del
NM_001127605.2:c.823-141del NP_001121077.1:n.823-141del
NM_001288979.1:c.475-141del NP_001275908.1:n.475-141del
XM_024448023.1:c.823-141del XP_024303791.1:n.823-141del
NM_000235.4:c.823-141del MANE Select NP_000226.2:n.823-141del
NM_001127605.3:c.823-141del NP_001121077.1:n.823-141del
NM_001288979.2:c.475-141del NP_001275908.1:n.475-141del