Canonical Allele Identifier: CA377517743
Community Standard Title: NM_000235.4(LIPA):c.419G>A (p.Trp140Ter)
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89228209C>T , CM000672.2:g.89228209C>T GRCh38
NC_000010.10:g.90987966C>T , CM000672.1:g.90987966C>T GRCh37
NC_000010.9:g.90977946C>T NCBI36
NG_008194.1:g.28695G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000235.4:c.419G>A MANE Select NP_000226.2:p.Trp140Ter
ENST00000336233.10:c.419G>A MANE Select ENSP00000337354.5:p.Trp140Ter
NM_000235.3:c.419G>A NP_000226.2:p.Trp140Ter
NM_001127605.2:c.419G>A NP_001121077.1:p.Trp140Ter
NM_001127605.3:c.419G>A NP_001121077.1:p.Trp140Ter
NM_001288979.1:c.71G>A NP_001275908.1:p.Trp24Ter
NM_001288979.2:c.71G>A NP_001275908.1:p.Trp24Ter
ENST00000282673.5:c.419G>A ENSP00000282673.4:p.Trp140Ter
ENST00000336233.9:c.419G>A ENSP00000337354.5:p.Trp140Ter
ENST00000371837.5:c.251G>A ENSP00000360903.1:p.Trp84Ter
ENST00000428800.5:c.419G>A ENSP00000388415.1:p.Trp140Ter
ENST00000456827.5:c.71G>A ENSP00000413019.2:p.Trp24Ter
XM_024448023.1:c.419G>A XP_024303791.1:p.Trp140Ter