Canonical Allele Identifier: CA5593565
Community Standard Title: NM_000235.4(LIPA):c.920C>A (p.Ala307Asp)
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89215984G>T , CM000672.2:g.89215984G>T GRCh38
NC_000010.10:g.90975741G>T , CM000672.1:g.90975741G>T GRCh37
NC_000010.9:g.90965721G>T NCBI36
NG_008194.1:g.40920C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000235.4:c.920C>A MANE Select NP_000226.2:p.Ala307Asp
ENST00000336233.10:c.920C>A MANE Select ENSP00000337354.5:p.Ala307Asp
NM_000235.3:c.920C>A NP_000226.2:p.Ala307Asp
NM_001127605.2:c.920C>A NP_001121077.1:p.Ala307Asp
NM_001127605.3:c.920C>A NP_001121077.1:p.Ala307Asp
NM_001288979.1:c.572C>A NP_001275908.1:p.Ala191Asp
NM_001288979.2:c.572C>A NP_001275908.1:p.Ala191Asp
ENST00000336233.9:c.920C>A ENSP00000337354.5:p.Ala307Asp
ENST00000371837.5:c.752C>A ENSP00000360903.1:p.Ala251Asp
ENST00000456827.5:c.572C>A ENSP00000413019.2:p.Ala191Asp
XM_024448023.1:c.920C>A XP_024303791.1:p.Ala307Asp