Canonical Allele Identifier: CA5593830

Gene: LIPA

Linked Data

• ClinVar Variation Id: 1113491
• ClinVar RCV Id: RCV001440895 ; RCV001826258 ; RCV002405036
• dbSNP Id: rs377437637
• ExAC: 10:91007330 G / A
• gnomAD v2: 10-91007330-G-A
• gnomAD v3: 10-89247573-G-A
• gnomAD v4: 10-89247573-G-A
• MyVariant Identifiers: chr10:g.91007330G>A (hg19) ; chr10:g.89247573G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89247573G>A , CM000672.2:g.89247573G>A	GRCh38
NC_000010.10:g.91007330G>A , CM000672.1:g.91007330G>A	GRCh37
NC_000010.9:g.90997310G>A	NCBI36
NG_008194.1:g.9331C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.76C>T MANE Select	ENSP00000337354.5:p.Leu26=
ENST00000282673.5:c.76C>T	ENSP00000282673.4:p.Leu26=
ENST00000336233.9:c.76C>T	ENSP00000337354.5:p.Leu26=
ENST00000371837.5:c.62-19175C>T	ENSP00000360903.1:n.62-19175C>T
ENST00000428800.5:c.76C>T	ENSP00000388415.1:p.Leu26=
ENST00000456827.5:c.-120+4164C>T	ENSP00000413019.2:n.-120+4164C>T
NM_000235.3:c.76C>T	NP_000226.2:p.Leu26=
NM_001127605.2:c.76C>T	NP_001121077.1:p.Leu26=
NM_001288979.1:c.-120+4164C>T	NP_001275908.1:n.-120+4164C>T
XM_024448023.1:c.76C>T	XP_024303791.1:p.Leu26=
NM_000235.4:c.76C>T MANE Select	NP_000226.2:p.Leu26=
NM_001127605.3:c.76C>T	NP_001121077.1:p.Leu26=
NM_001288979.2:c.-120+4164C>T	NP_001275908.1:n.-120+4164C>T