Canonical Allele Identifier: CA1926746360
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89243390_89243391delinsAC , CM000672.2:g.89243390_89243391delinsAC GRCh38
NC_000010.10:g.91003147_91003148delinsAC , CM000672.1:g.91003147_91003148delinsAC GRCh37
NC_000010.9:g.90993127_90993128delinsAC NCBI36
NG_008194.1:g.13513_13514delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.229+2285_229+2286delinsGT MANE Select ENSP00000337354.5:n.229+2285_229+2286delinsGT
ENST00000282673.5:c.229+2285_229+2286delinsGT ENSP00000282673.4:n.229+2285_229+2286delinsGT
ENST00000336233.9:c.229+2285_229+2286delinsGT ENSP00000337354.5:n.229+2285_229+2286delinsGT
ENST00000371837.5:c.62-14993_62-14992delinsGT ENSP00000360903.1:n.62-14993_62-14992delinsGT
ENST00000428800.5:c.229+2285_229+2286delinsGT ENSP00000388415.1:n.229+2285_229+2286delinsGT
ENST00000456827.5:c.-120+8346_-120+8347delinsGT ENSP00000413019.2:n.-120+8346_-120+8347delinsGT
NM_000235.3:c.229+2285_229+2286delinsGT NP_000226.2:n.229+2285_229+2286delinsGT
NM_001127605.2:c.229+2285_229+2286delinsGT NP_001121077.1:n.229+2285_229+2286delinsGT
NM_001288979.1:c.-120+8346_-120+8347delinsGT NP_001275908.1:n.-120+8346_-120+8347delinsGT
XM_024448023.1:c.229+2285_229+2286delinsGT XP_024303791.1:n.229+2285_229+2286delinsGT
NM_000235.4:c.229+2285_229+2286delinsGT MANE Select NP_000226.2:n.229+2285_229+2286delinsGT
NM_001127605.3:c.229+2285_229+2286delinsGT NP_001121077.1:n.229+2285_229+2286delinsGT
NM_001288979.2:c.-120+8346_-120+8347delinsGT NP_001275908.1:n.-120+8346_-120+8347delinsGT