Canonical Allele Identifier: CA2610082470
Gene: LIPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89247843_89247865del , CM000672.2:g.89247843_89247865del GRCh38
NC_000010.10:g.91007600_91007622del , CM000672.1:g.91007600_91007622del GRCh37
NC_000010.9:g.90997580_90997602del NCBI36
NG_008194.1:g.9054_9076del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.-1-201_-1-179del MANE Select ENSP00000337354.5:n.-1-201_-1-179del
ENST00000282673.5:c.-1-201_-1-179del ENSP00000282673.4:n.-1-201_-1-179del
ENST00000336233.9:c.-1-201_-1-179del ENSP00000337354.5:n.-1-201_-1-179del
ENST00000371837.5:c.62-19452_62-19430del ENSP00000360903.1:n.62-19452_62-19430del
ENST00000456827.5:c.-120+3887_-120+3909del ENSP00000413019.2:n.-120+3887_-120+3909del
NM_000235.3:c.-1-201_-1-179del NP_000226.2:n.-1-201_-1-179del
NM_001127605.2:c.-1-201_-1-179del NP_001121077.1:n.-1-201_-1-179del
NM_001288979.1:c.-120+3887_-120+3909del NP_001275908.1:n.-120+3887_-120+3909del
XM_024448023.1:c.-1-201_-1-179del XP_024303791.1:n.-1-201_-1-179del
NM_000235.4:c.-1-201_-1-179del MANE Select NP_000226.2:n.-1-201_-1-179del
NM_001127605.3:c.-1-201_-1-179del NP_001121077.1:n.-1-201_-1-179del
NM_001288979.2:c.-120+3887_-120+3909del NP_001275908.1:n.-120+3887_-120+3909del