Canonical Allele Identifier: CA5593508

Gene: LIPA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89214922A>G , CM000672.2:g.89214922A>G	GRCh38
NC_000010.10:g.90974679A>G , CM000672.1:g.90974679A>G	GRCh37
NC_000010.9:g.90964659A>G	NCBI36
NG_008194.1:g.41982T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000235.4:c.1106T>C MANE Select	NP_000226.2:p.Ile369Thr
ENST00000336233.10:c.1106T>C MANE Select	ENSP00000337354.5:p.Ile369Thr
NM_000235.3:c.1106T>C	NP_000226.2:p.Ile369Thr
NM_001127605.2:c.1106T>C	NP_001121077.1:p.Ile369Thr
NM_001127605.3:c.1106T>C	NP_001121077.1:p.Ile369Thr
NM_001288979.1:c.758T>C	NP_001275908.1:p.Ile253Thr
NM_001288979.2:c.758T>C	NP_001275908.1:p.Ile253Thr
ENST00000336233.9:c.1106T>C	ENSP00000337354.5:p.Ile369Thr
ENST00000371837.5:c.938T>C	ENSP00000360903.1:p.Ile313Thr
ENST00000456827.5:c.758T>C	ENSP00000413019.2:p.Ile253Thr
XM_024448023.1:c.1106T>C	XP_024303791.1:p.Ile369Thr