Canonical Allele Identifier: CA2610081909
Gene: LIPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89247410_89247411insTTAAT , CM000672.2:g.89247410_89247411insTTAAT GRCh38
NC_000010.10:g.91007167_91007168insTTAAT , CM000672.1:g.91007167_91007168insTTAAT GRCh37
NC_000010.9:g.90997147_90997148insTTAAT NCBI36
NG_008194.1:g.9493_9494insATTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.111+127_111+128insATTAA MANE Select ENSP00000337354.5:n.111+127_111+128insATTAA
ENST00000282673.5:c.111+127_111+128insATTAA ENSP00000282673.4:n.111+127_111+128insATTAA
ENST00000336233.9:c.111+127_111+128insATTAA ENSP00000337354.5:n.111+127_111+128insATTAA
ENST00000371837.5:c.62-19013_62-19012insATTAA ENSP00000360903.1:n.62-19013_62-19012insATTAA
ENST00000428800.5:c.111+127_111+128insATTAA ENSP00000388415.1:n.111+127_111+128insATTAA
ENST00000456827.5:c.-120+4326_-120+4327insATTAA ENSP00000413019.2:n.-120+4326_-120+4327insATTAA
NM_000235.3:c.111+127_111+128insATTAA NP_000226.2:n.111+127_111+128insATTAA
NM_001127605.2:c.111+127_111+128insATTAA NP_001121077.1:n.111+127_111+128insATTAA
NM_001288979.1:c.-120+4326_-120+4327insATTAA NP_001275908.1:n.-120+4326_-120+4327insATTAA
XM_024448023.1:c.111+127_111+128insATTAA XP_024303791.1:n.111+127_111+128insATTAA
NM_000235.4:c.111+127_111+128insATTAA MANE Select NP_000226.2:n.111+127_111+128insATTAA
NM_001127605.3:c.111+127_111+128insATTAA NP_001121077.1:n.111+127_111+128insATTAA
NM_001288979.2:c.-120+4326_-120+4327insATTAA NP_001275908.1:n.-120+4326_-120+4327insATTAA