Canonical Allele Identifier: CA377516636

Gene: LIPA

Linked Data

• MyVariant Identifiers: chr10:g.90982268C>A (hg19) ; chr10:g.89222511C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89222511C>A , CM000672.2:g.89222511C>A	GRCh38
NC_000010.10:g.90982268C>A , CM000672.1:g.90982268C>A	GRCh37
NC_000010.9:g.90972248C>A	NCBI36
NG_008194.1:g.34393G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336233.10:c.894G>T MANE Select	ENSP00000337354.5:p.Gln298His
ENST00000336233.9:c.894G>T	ENSP00000337354.5:p.Gln298His
ENST00000371837.5:c.726G>T	ENSP00000360903.1:p.Gln242His
ENST00000456827.5:c.546G>T	ENSP00000413019.2:p.Gln182His
NM_000235.3:c.894G>T	NP_000226.2:p.Gln298His
NM_001127605.2:c.894G>T	NP_001121077.1:p.Gln298His
NM_001288979.1:c.546G>T	NP_001275908.1:p.Gln182His
XM_024448023.1:c.894G>T	XP_024303791.1:p.Gln298His
NM_000235.4:c.894G>T MANE Select	NP_000226.2:p.Gln298His
NM_001127605.3:c.894G>T	NP_001121077.1:p.Gln298His
NM_001288979.2:c.546G>T	NP_001275908.1:p.Gln182His