Canonical Allele Identifier: CA1926733114

Gene: LIPA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89222514G= , CM000672.2:g.89222514G=	GRCh38
NC_000010.10:g.90982271G= , CM000672.1:g.90982271G=	GRCh37
NC_000010.9:g.90972251G=	NCBI36
NG_008194.1:g.34390C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336233.10:c.891C= MANE Select	ENSP00000337354.5:p.Ser297=
ENST00000336233.9:c.891C=	ENSP00000337354.5:p.Ser297=
ENST00000371837.5:c.723C=	ENSP00000360903.1:p.Ser241=
ENST00000456827.5:c.543C=	ENSP00000413019.2:p.Ser181=
NM_000235.3:c.891C=	NP_000226.2:p.Ser297=
NM_001127605.2:c.891C=	NP_001121077.1:p.Ser297=
NM_001288979.1:c.543C=	NP_001275908.1:p.Ser181=
XM_024448023.1:c.891C=	XP_024303791.1:p.Ser297=
NM_000235.4:c.891C= MANE Select	NP_000226.2:p.Ser297=
NM_001127605.3:c.891C=	NP_001121077.1:p.Ser297=
NM_001288979.2:c.543C=	NP_001275908.1:p.Ser181=