Canonical Allele Identifier: CA2574617153
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89247689del , CM000672.2:g.89247689del GRCh38
NC_000010.10:g.91007446del , CM000672.1:g.91007446del GRCh37
NC_000010.9:g.90997426del NCBI36
NG_008194.1:g.9218del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.-1-37del MANE Select ENSP00000337354.5:n.-1-37del
ENST00000282673.5:c.-1-37del ENSP00000282673.4:n.-1-37del
ENST00000336233.9:c.-1-37del ENSP00000337354.5:n.-1-37del
ENST00000371837.5:c.62-19288del ENSP00000360903.1:n.62-19288del
ENST00000428800.5:c.-38del ENSP00000388415.1:n.-38del
ENST00000456827.5:c.-120+4051del ENSP00000413019.2:n.-120+4051del
NM_000235.3:c.-1-37del NP_000226.2:n.-1-37del
NM_001127605.2:c.-1-37del NP_001121077.1:n.-1-37del
NM_001288979.1:c.-120+4051del NP_001275908.1:n.-120+4051del
XM_024448023.1:c.-1-37del XP_024303791.1:n.-1-37del
NM_000235.4:c.-1-37del MANE Select NP_000226.2:n.-1-37del
NM_001127605.3:c.-1-37del NP_001121077.1:n.-1-37del
NM_001288979.2:c.-120+4051del NP_001275908.1:n.-120+4051del