Canonical Allele Identifier: CA377518406

Gene: LIPA

Linked Data

• gnomAD v4: 10-89245784-T-C
• MyVariant Identifiers: chr10:g.91005541T>C (hg19) ; chr10:g.89245784T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89245784T>C , CM000672.2:g.89245784T>C	GRCh38
NC_000010.10:g.91005541T>C , CM000672.1:g.91005541T>C	GRCh37
NC_000010.9:g.90995521T>C	NCBI36
NG_008194.1:g.11120A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.121A>G MANE Select	ENSP00000337354.5:p.Ile41Val
ENST00000282673.5:c.121A>G	ENSP00000282673.4:p.Ile41Val
ENST00000336233.9:c.121A>G	ENSP00000337354.5:p.Ile41Val
ENST00000371837.5:c.62-17386A>G	ENSP00000360903.1:n.62-17386A>G
ENST00000428800.5:c.121A>G	ENSP00000388415.1:p.Ile41Val
ENST00000456827.5:c.-120+5953A>G	ENSP00000413019.2:n.-120+5953A>G
NM_000235.3:c.121A>G	NP_000226.2:p.Ile41Val
NM_001127605.2:c.121A>G	NP_001121077.1:p.Ile41Val
NM_001288979.1:c.-120+5953A>G	NP_001275908.1:n.-120+5953A>G
XM_024448023.1:c.121A>G	XP_024303791.1:p.Ile41Val
NM_000235.4:c.121A>G MANE Select	NP_000226.2:p.Ile41Val
NM_001127605.3:c.121A>G	NP_001121077.1:p.Ile41Val
NM_001288979.2:c.-120+5953A>G	NP_001275908.1:n.-120+5953A>G