Canonical Allele Identifier: CA2610082455
Gene: LIPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89247843_89247861del , CM000672.2:g.89247843_89247861del GRCh38
NC_000010.10:g.91007600_91007618del , CM000672.1:g.91007600_91007618del GRCh37
NC_000010.9:g.90997580_90997598del NCBI36
NG_008194.1:g.9060_9078del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.-1-195_-1-177del MANE Select ENSP00000337354.5:n.-1-195_-1-177del
ENST00000282673.5:c.-1-195_-1-177del ENSP00000282673.4:n.-1-195_-1-177del
ENST00000336233.9:c.-1-195_-1-177del ENSP00000337354.5:n.-1-195_-1-177del
ENST00000371837.5:c.62-19446_62-19428del ENSP00000360903.1:n.62-19446_62-19428del
ENST00000456827.5:c.-120+3893_-120+3911del ENSP00000413019.2:n.-120+3893_-120+3911del
NM_000235.3:c.-1-195_-1-177del NP_000226.2:n.-1-195_-1-177del
NM_001127605.2:c.-1-195_-1-177del NP_001121077.1:n.-1-195_-1-177del
NM_001288979.1:c.-120+3893_-120+3911del NP_001275908.1:n.-120+3893_-120+3911del
XM_024448023.1:c.-1-195_-1-177del XP_024303791.1:n.-1-195_-1-177del
NM_000235.4:c.-1-195_-1-177del MANE Select NP_000226.2:n.-1-195_-1-177del
NM_001127605.3:c.-1-195_-1-177del NP_001121077.1:n.-1-195_-1-177del
NM_001288979.2:c.-120+3893_-120+3911del NP_001275908.1:n.-120+3893_-120+3911del