Canonical Allele Identifier: CA2522951076
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89222645_89222647del , CM000672.2:g.89222645_89222647del GRCh38
NC_000010.10:g.90982402_90982404del , CM000672.1:g.90982402_90982404del GRCh37
NC_000010.9:g.90972382_90972384del NCBI36
NG_008194.1:g.34257_34259del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.823-65_823-63del MANE Select ENSP00000337354.5:n.823-65_823-63del
ENST00000336233.9:c.823-65_823-63del ENSP00000337354.5:n.823-65_823-63del
ENST00000371837.5:c.655-65_655-63del ENSP00000360903.1:n.655-65_655-63del
ENST00000428800.5:c.823-65_823-63del ENSP00000388415.1:n.823-65_823-63del
ENST00000456827.5:c.475-65_475-63del ENSP00000413019.2:n.475-65_475-63del
NM_000235.3:c.823-65_823-63del NP_000226.2:n.823-65_823-63del
NM_001127605.2:c.823-65_823-63del NP_001121077.1:n.823-65_823-63del
NM_001288979.1:c.475-65_475-63del NP_001275908.1:n.475-65_475-63del
XM_024448023.1:c.823-65_823-63del XP_024303791.1:n.823-65_823-63del
NM_000235.4:c.823-65_823-63del MANE Select NP_000226.2:n.823-65_823-63del
NM_001127605.3:c.823-65_823-63del NP_001121077.1:n.823-65_823-63del
NM_001288979.2:c.475-65_475-63del NP_001275908.1:n.475-65_475-63del