Canonical Allele Identifier: CA377516742
Gene: LIPA HGNC NCBI

Linked Data

dbSNP Id: rs1842713812

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89222558G>A , CM000672.2:g.89222558G>A GRCh38
NC_000010.10:g.90982315G>A , CM000672.1:g.90982315G>A GRCh37
NC_000010.9:g.90972295G>A NCBI36
NG_008194.1:g.34346C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.847C>T MANE Select ENSP00000337354.5:p.His283Tyr
ENST00000336233.9:c.847C>T ENSP00000337354.5:p.His283Tyr
ENST00000371837.5:c.679C>T ENSP00000360903.1:p.His227Tyr
ENST00000428800.5:c.847C>T ENSP00000388415.1:p.His283Tyr
ENST00000456827.5:c.499C>T ENSP00000413019.2:p.His167Tyr
NM_000235.3:c.847C>T NP_000226.2:p.His283Tyr
NM_001127605.2:c.847C>T NP_001121077.1:p.His283Tyr
NM_001288979.1:c.499C>T NP_001275908.1:p.His167Tyr
XM_024448023.1:c.847C>T XP_024303791.1:p.His283Tyr
NM_000235.4:c.847C>T MANE Select NP_000226.2:p.His283Tyr
NM_001127605.3:c.847C>T NP_001121077.1:p.His283Tyr
NM_001288979.2:c.499C>T NP_001275908.1:p.His167Tyr