Canonical Allele Identifier: CA1926733079

Gene: LIPA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89222443G= , CM000672.2:g.89222443G=	GRCh38
NC_000010.10:g.90982200G= , CM000672.1:g.90982200G=	GRCh37
NC_000010.9:g.90972180G=	NCBI36
NG_008194.1:g.34461C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.894+68C= MANE Select	ENSP00000337354.5:n.894+68C=
ENST00000336233.9:c.894+68C=	ENSP00000337354.5:n.894+68C=
ENST00000371837.5:c.726+68C=	ENSP00000360903.1:n.726+68C=
ENST00000456827.5:c.546+68C=	ENSP00000413019.2:n.546+68C=
NM_000235.3:c.894+68C=	NP_000226.2:n.894+68C=
NM_001127605.2:c.894+68C=	NP_001121077.1:n.894+68C=
NM_001288979.1:c.546+68C=	NP_001275908.1:n.546+68C=
XM_024448023.1:c.894+68C=	XP_024303791.1:n.894+68C=
NM_000235.4:c.894+68C= MANE Select	NP_000226.2:n.894+68C=
NM_001127605.3:c.894+68C=	NP_001121077.1:n.894+68C=
NM_001288979.2:c.546+68C=	NP_001275908.1:n.546+68C=