Canonical Allele Identifier: CA5593499
Community Standard Title: NM_000235.4(LIPA):c.1158G>T (p.Arg386Ser)
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89214870C>A , CM000672.2:g.89214870C>A GRCh38
NC_000010.10:g.90974627C>A , CM000672.1:g.90974627C>A GRCh37
NC_000010.9:g.90964607C>A NCBI36
NG_008194.1:g.42034G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000235.4:c.1158G>T MANE Select NP_000226.2:p.Arg386Ser
ENST00000336233.10:c.1158G>T MANE Select ENSP00000337354.5:p.Arg386Ser
NM_000235.3:c.1158G>T NP_000226.2:p.Arg386Ser
NM_001127605.2:c.1158G>T NP_001121077.1:p.Arg386Ser
NM_001127605.3:c.1158G>T NP_001121077.1:p.Arg386Ser
NM_001288979.1:c.810G>T NP_001275908.1:p.Arg270Ser
NM_001288979.2:c.810G>T NP_001275908.1:p.Arg270Ser
ENST00000336233.9:c.1158G>T ENSP00000337354.5:p.Arg386Ser
ENST00000371837.5:c.990G>T ENSP00000360903.1:p.Arg330Ser
ENST00000456827.5:c.810G>T ENSP00000413019.2:p.Arg270Ser
XM_024448023.1:c.1158G>T XP_024303791.1:p.Arg386Ser