Canonical Allele Identifier: CA377516757
Gene: LIPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89222565A>T , CM000672.2:g.89222565A>T GRCh38
NC_000010.10:g.90982322A>T , CM000672.1:g.90982322A>T GRCh37
NC_000010.9:g.90972302A>T NCBI36
NG_008194.1:g.34339T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.840T>A MANE Select ENSP00000337354.5:p.Tyr280Ter
ENST00000336233.9:c.840T>A ENSP00000337354.5:p.Tyr280Ter
ENST00000371837.5:c.672T>A ENSP00000360903.1:p.Tyr224Ter
ENST00000428800.5:c.840T>A ENSP00000388415.1:p.Tyr280Ter
ENST00000456827.5:c.492T>A ENSP00000413019.2:p.Tyr164Ter
NM_000235.3:c.840T>A NP_000226.2:p.Tyr280Ter
NM_001127605.2:c.840T>A NP_001121077.1:p.Tyr280Ter
NM_001288979.1:c.492T>A NP_001275908.1:p.Tyr164Ter
XM_024448023.1:c.840T>A XP_024303791.1:p.Tyr280Ter
NM_000235.4:c.840T>A MANE Select NP_000226.2:p.Tyr280Ter
NM_001127605.3:c.840T>A NP_001121077.1:p.Tyr280Ter
NM_001288979.2:c.492T>A NP_001275908.1:p.Tyr164Ter