Canonical Allele Identifier: CA2610080831

Gene: LIPA

Linked Data

• gnomAD v4: 10-89222627-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89222627G>A , CM000672.2:g.89222627G>A	GRCh38
NC_000010.10:g.90982384G>A , CM000672.1:g.90982384G>A	GRCh37
NC_000010.9:g.90972364G>A	NCBI36
NG_008194.1:g.34277C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.823-45C>T MANE Select	ENSP00000337354.5:n.823-45C>T
ENST00000336233.9:c.823-45C>T	ENSP00000337354.5:n.823-45C>T
ENST00000371837.5:c.655-45C>T	ENSP00000360903.1:n.655-45C>T
ENST00000428800.5:c.823-45C>T	ENSP00000388415.1:n.823-45C>T
ENST00000456827.5:c.475-45C>T	ENSP00000413019.2:n.475-45C>T
NM_000235.3:c.823-45C>T	NP_000226.2:n.823-45C>T
NM_001127605.2:c.823-45C>T	NP_001121077.1:n.823-45C>T
NM_001288979.1:c.475-45C>T	NP_001275908.1:n.475-45C>T
XM_024448023.1:c.823-45C>T	XP_024303791.1:n.823-45C>T
NM_000235.4:c.823-45C>T MANE Select	NP_000226.2:n.823-45C>T
NM_001127605.3:c.823-45C>T	NP_001121077.1:n.823-45C>T
NM_001288979.2:c.475-45C>T	NP_001275908.1:n.475-45C>T