Canonical Allele Identifier: CA2788926351

Gene: LIPA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89247385_89247386insT , CM000672.2:g.89247385_89247386insT	GRCh38
NC_000010.10:g.91007142_91007143insT , CM000672.1:g.91007142_91007143insT	GRCh37
NC_000010.9:g.90997122_90997123insT	NCBI36
NG_008194.1:g.9518_9519insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.111+152_111+153insA MANE Select	ENSP00000337354.5:n.111+152_111+153insA
ENST00000282673.5:c.111+152_111+153insA	ENSP00000282673.4:n.111+152_111+153insA
ENST00000336233.9:c.111+152_111+153insA	ENSP00000337354.5:n.111+152_111+153insA
ENST00000371837.5:c.62-18988_62-18987insA	ENSP00000360903.1:n.62-18988_62-18987insA
ENST00000428800.5:c.111+152_111+153insA	ENSP00000388415.1:n.111+152_111+153insA
ENST00000456827.5:c.-120+4351_-120+4352insA	ENSP00000413019.2:n.-120+4351_-120+4352insA
NM_000235.3:c.111+152_111+153insA	NP_000226.2:n.111+152_111+153insA
NM_001127605.2:c.111+152_111+153insA	NP_001121077.1:n.111+152_111+153insA
NM_001288979.1:c.-120+4351_-120+4352insA	NP_001275908.1:n.-120+4351_-120+4352insA
XM_024448023.1:c.111+152_111+153insA	XP_024303791.1:n.111+152_111+153insA
NM_000235.4:c.111+152_111+153insA MANE Select	NP_000226.2:n.111+152_111+153insA
NM_001127605.3:c.111+152_111+153insA	NP_001121077.1:n.111+152_111+153insA
NM_001288979.2:c.-120+4351_-120+4352insA	NP_001275908.1:n.-120+4351_-120+4352insA