Canonical Allele Identifier: CA377516651

Gene: LIPA

Linked Data

• MyVariant Identifiers: chr10:g.90982274C>T (hg19) ; chr10:g.89222517C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89222517C>T , CM000672.2:g.89222517C>T	GRCh38
NC_000010.10:g.90982274C>T , CM000672.1:g.90982274C>T	GRCh37
NC_000010.9:g.90972254C>T	NCBI36
NG_008194.1:g.34387G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.888G>A MANE Select	ENSP00000337354.5:p.Trp296Ter
ENST00000336233.9:c.888G>A	ENSP00000337354.5:p.Trp296Ter
ENST00000371837.5:c.720G>A	ENSP00000360903.1:p.Trp240Ter
ENST00000456827.5:c.540G>A	ENSP00000413019.2:p.Trp180Ter
NM_000235.3:c.888G>A	NP_000226.2:p.Trp296Ter
NM_001127605.2:c.888G>A	NP_001121077.1:p.Trp296Ter
NM_001288979.1:c.540G>A	NP_001275908.1:p.Trp180Ter
XM_024448023.1:c.888G>A	XP_024303791.1:p.Trp296Ter
NM_000235.4:c.888G>A MANE Select	NP_000226.2:p.Trp296Ter
NM_001127605.3:c.888G>A	NP_001121077.1:p.Trp296Ter
NM_001288979.2:c.540G>A	NP_001275908.1:p.Trp180Ter