Canonical Allele Identifier: CA669697916

Gene: LIPA

Linked Data

• dbSNP Id: rs1282349617
• MyVariant Identifiers: chr10:g.91007497C>G (hg19) ; chr10:g.89247740C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89247740C>G , CM000672.2:g.89247740C>G	GRCh38
NC_000010.10:g.91007497C>G , CM000672.1:g.91007497C>G	GRCh37
NC_000010.9:g.90997477C>G	NCBI36
NG_008194.1:g.9164G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.-1-91G>C MANE Select	ENSP00000337354.5:n.-1-91G>C
ENST00000282673.5:c.-1-91G>C	ENSP00000282673.4:n.-1-91G>C
ENST00000336233.9:c.-1-91G>C	ENSP00000337354.5:n.-1-91G>C
ENST00000371837.5:c.62-19342G>C	ENSP00000360903.1:n.62-19342G>C
ENST00000428800.5:c.-92G>C	ENSP00000388415.1:n.-92G>C
ENST00000456827.5:c.-120+3997G>C	ENSP00000413019.2:n.-120+3997G>C
NM_000235.3:c.-1-91G>C	NP_000226.2:n.-1-91G>C
NM_001127605.2:c.-1-91G>C	NP_001121077.1:n.-1-91G>C
NM_001288979.1:c.-120+3997G>C	NP_001275908.1:n.-120+3997G>C
XM_024448023.1:c.-1-91G>C	XP_024303791.1:n.-1-91G>C
NM_000235.4:c.-1-91G>C MANE Select	NP_000226.2:n.-1-91G>C
NM_001127605.3:c.-1-91G>C	NP_001121077.1:n.-1-91G>C
NM_001288979.2:c.-120+3997G>C	NP_001275908.1:n.-120+3997G>C