Canonical Allele Identifier: CA2610082456

Gene: LIPA

Linked Data

• gnomAD v4: 10-89247825-A-AATTTTATTTATTTATTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89247843_89247861dup , CM000672.2:g.89247843_89247861dup	GRCh38
NC_000010.10:g.91007600_91007618dup , CM000672.1:g.91007600_91007618dup	GRCh37
NC_000010.9:g.90997580_90997598dup	NCBI36
NG_008194.1:g.9060_9078dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.-1-195_-1-177dup MANE Select	ENSP00000337354.5:n.-1-195_-1-177dup
ENST00000282673.5:c.-1-195_-1-177dup	ENSP00000282673.4:n.-1-195_-1-177dup
ENST00000336233.9:c.-1-195_-1-177dup	ENSP00000337354.5:n.-1-195_-1-177dup
ENST00000371837.5:c.62-19446_62-19428dup	ENSP00000360903.1:n.62-19446_62-19428dup
ENST00000456827.5:c.-120+3893_-120+3911dup	ENSP00000413019.2:n.-120+3893_-120+3911dup
NM_000235.3:c.-1-195_-1-177dup	NP_000226.2:n.-1-195_-1-177dup
NM_001127605.2:c.-1-195_-1-177dup	NP_001121077.1:n.-1-195_-1-177dup
NM_001288979.1:c.-120+3893_-120+3911dup	NP_001275908.1:n.-120+3893_-120+3911dup
XM_024448023.1:c.-1-195_-1-177dup	XP_024303791.1:n.-1-195_-1-177dup
NM_000235.4:c.-1-195_-1-177dup MANE Select	NP_000226.2:n.-1-195_-1-177dup
NM_001127605.3:c.-1-195_-1-177dup	NP_001121077.1:n.-1-195_-1-177dup
NM_001288979.2:c.-120+3893_-120+3911dup	NP_001275908.1:n.-120+3893_-120+3911dup