Canonical Allele Identifier: CA669690051

Gene: LIPA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89229352T>A , CM000672.2:g.89229352T>A	GRCh38
NC_000010.10:g.90989109T>A , CM000672.1:g.90989109T>A	GRCh37
NC_000010.9:g.90979089T>A	NCBI36
NG_008194.1:g.27552A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.230-954A>T MANE Select	ENSP00000337354.5:n.230-954A>T
ENST00000282673.5:c.230-954A>T	ENSP00000282673.4:n.230-954A>T
ENST00000336233.9:c.230-954A>T	ENSP00000337354.5:n.230-954A>T
ENST00000371837.5:c.62-954A>T	ENSP00000360903.1:n.62-954A>T
ENST00000428800.5:c.230-954A>T	ENSP00000388415.1:n.230-954A>T
ENST00000456827.5:c.-119-954A>T	ENSP00000413019.2:n.-119-954A>T
NM_000235.3:c.230-954A>T	NP_000226.2:n.230-954A>T
NM_001127605.2:c.230-954A>T	NP_001121077.1:n.230-954A>T
NM_001288979.1:c.-119-954A>T	NP_001275908.1:n.-119-954A>T
XM_024448023.1:c.230-954A>T	XP_024303791.1:n.230-954A>T
NM_000235.4:c.230-954A>T MANE Select	NP_000226.2:n.230-954A>T
NM_001127605.3:c.230-954A>T	NP_001121077.1:n.230-954A>T
NM_001288979.2:c.-119-954A>T	NP_001275908.1:n.-119-954A>T