Canonical Allele Identifier: CA1926729481

Gene: LIPA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89213937C= , CM000672.2:g.89213937C=	GRCh38
NC_000010.10:g.90973694C= , CM000672.1:g.90973694C=	GRCh37
NC_000010.9:g.90963674C=	NCBI36
NG_008194.1:g.42967G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336233.10:c.*891G= MANE Select	ENSP00000337354.5:n.*891G=
ENST00000336233.9:c.*891G=	ENSP00000337354.5:n.*891G=
ENST00000371837.5:c.*891G=	ENSP00000360903.1:n.*891G=
ENST00000456827.5:c.*891G=	ENSP00000413019.2:n.*891G=
NM_000235.3:c.*891G=	NP_000226.2:n.*891G=
NM_001127605.2:c.*891G=	NP_001121077.1:n.*891G=
NM_001288979.1:c.*891G=	NP_001275908.1:n.*891G=
XM_024448023.1:c.*891G=	XP_024303791.1:n.*891G=
NM_000235.4:c.*891G= MANE Select	NP_000226.2:n.*891G=
NM_001127605.3:c.*891G=	NP_001121077.1:n.*891G=
NM_001288979.2:c.*891G=	NP_001275908.1:n.*891G=