Canonical Allele Identifier: CA5593751
Community Standard Title: NM_000235.4(LIPA):c.380G>A (p.Arg127Gln)
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89228248C>T , CM000672.2:g.89228248C>T GRCh38
NC_000010.10:g.90988005C>T , CM000672.1:g.90988005C>T GRCh37
NC_000010.9:g.90977985C>T NCBI36
NG_008194.1:g.28656G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000235.4:c.380G>A MANE Select NP_000226.2:p.Arg127Gln
ENST00000336233.10:c.380G>A MANE Select ENSP00000337354.5:p.Arg127Gln
NM_000235.3:c.380G>A NP_000226.2:p.Arg127Gln
NM_001127605.2:c.380G>A NP_001121077.1:p.Arg127Gln
NM_001127605.3:c.380G>A NP_001121077.1:p.Arg127Gln
NM_001288979.1:c.32G>A NP_001275908.1:p.Arg11Gln
NM_001288979.2:c.32G>A NP_001275908.1:p.Arg11Gln
ENST00000282673.5:c.380G>A ENSP00000282673.4:p.Arg127Gln
ENST00000336233.9:c.380G>A ENSP00000337354.5:p.Arg127Gln
ENST00000371837.5:c.212G>A ENSP00000360903.1:p.Arg71Gln
ENST00000428800.5:c.380G>A ENSP00000388415.1:p.Arg127Gln
ENST00000456827.5:c.32G>A ENSP00000413019.2:p.Arg11Gln
XM_024448023.1:c.380G>A XP_024303791.1:p.Arg127Gln