Canonical Allele Identifier: CA669697967

Gene: LIPA

Linked Data

• dbSNP Id: rs1225085937
• MyVariant Identifiers: chr10:g.91007595_91007607del (hg19) ; chr10:g.89247838_89247850del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89247839_89247851del , CM000672.2:g.89247839_89247851del	GRCh38
NC_000010.10:g.91007596_91007608del , CM000672.1:g.91007596_91007608del	GRCh37
NC_000010.9:g.90997576_90997588del	NCBI36
NG_008194.1:g.9054_9066del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.-1-201_-1-189del MANE Select	ENSP00000337354.5:n.-1-201_-1-189del
ENST00000282673.5:c.-1-201_-1-189del	ENSP00000282673.4:n.-1-201_-1-189del
ENST00000336233.9:c.-1-201_-1-189del	ENSP00000337354.5:n.-1-201_-1-189del
ENST00000371837.5:c.62-19452_62-19440del	ENSP00000360903.1:n.62-19452_62-19440del
ENST00000456827.5:c.-120+3887_-120+3899del	ENSP00000413019.2:n.-120+3887_-120+3899del
NM_000235.3:c.-1-201_-1-189del	NP_000226.2:n.-1-201_-1-189del
NM_001127605.2:c.-1-201_-1-189del	NP_001121077.1:n.-1-201_-1-189del
NM_001288979.1:c.-120+3887_-120+3899del	NP_001275908.1:n.-120+3887_-120+3899del
XM_024448023.1:c.-1-201_-1-189del	XP_024303791.1:n.-1-201_-1-189del
NM_000235.4:c.-1-201_-1-189del MANE Select	NP_000226.2:n.-1-201_-1-189del
NM_001127605.3:c.-1-201_-1-189del	NP_001121077.1:n.-1-201_-1-189del
NM_001288979.2:c.-120+3887_-120+3899del	NP_001275908.1:n.-120+3887_-120+3899del