Canonical Allele Identifier: CA2610080647

Gene: LIPA

Linked Data

• gnomAD v4: 10-89222477-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89222477A>G , CM000672.2:g.89222477A>G	GRCh38
NC_000010.10:g.90982234A>G , CM000672.1:g.90982234A>G	GRCh37
NC_000010.9:g.90972214A>G	NCBI36
NG_008194.1:g.34427T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.894+34T>C MANE Select	ENSP00000337354.5:n.894+34T>C
ENST00000336233.9:c.894+34T>C	ENSP00000337354.5:n.894+34T>C
ENST00000371837.5:c.726+34T>C	ENSP00000360903.1:n.726+34T>C
ENST00000456827.5:c.546+34T>C	ENSP00000413019.2:n.546+34T>C
NM_000235.3:c.894+34T>C	NP_000226.2:n.894+34T>C
NM_001127605.2:c.894+34T>C	NP_001121077.1:n.894+34T>C
NM_001288979.1:c.546+34T>C	NP_001275908.1:n.546+34T>C
XM_024448023.1:c.894+34T>C	XP_024303791.1:n.894+34T>C
NM_000235.4:c.894+34T>C MANE Select	NP_000226.2:n.894+34T>C
NM_001127605.3:c.894+34T>C	NP_001121077.1:n.894+34T>C
NM_001288979.2:c.546+34T>C	NP_001275908.1:n.546+34T>C