Canonical Allele Identifier: CA2610081682

Gene: LIPA

Linked Data

• gnomAD v4: 10-89245777-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89245779del , CM000672.2:g.89245779del	GRCh38
NC_000010.10:g.91005536del , CM000672.1:g.91005536del	GRCh37
NC_000010.9:g.90995516del	NCBI36
NG_008194.1:g.11126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.127del MANE Select	ENSP00000337354.5:p.Tyr43ThrfsTer10
ENST00000282673.5:c.127del	ENSP00000282673.4:p.Tyr43ThrfsTer10
ENST00000336233.9:c.127del	ENSP00000337354.5:p.Tyr43ThrfsTer10
ENST00000371837.5:c.62-17380del	ENSP00000360903.1:n.62-17380del
ENST00000428800.5:c.127del	ENSP00000388415.1:p.Tyr43ThrfsTer10
ENST00000456827.5:c.-120+5959del	ENSP00000413019.2:n.-120+5959del
NM_000235.3:c.127del	NP_000226.2:p.Tyr43ThrfsTer10
NM_001127605.2:c.127del	NP_001121077.1:p.Tyr43ThrfsTer10
NM_001288979.1:c.-120+5959del	NP_001275908.1:n.-120+5959del
XM_024448023.1:c.127del	XP_024303791.1:p.Tyr43ThrfsTer10
NM_000235.4:c.127del MANE Select	NP_000226.2:p.Tyr43ThrfsTer10
NM_001127605.3:c.127del	NP_001121077.1:p.Tyr43ThrfsTer10
NM_001288979.2:c.-120+5959del	NP_001275908.1:n.-120+5959del