Canonical Allele Identifier: CA1926729460
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89213879G= , CM000672.2:g.89213879G= GRCh38
NC_000010.10:g.90973636G= , CM000672.1:g.90973636G= GRCh37
NC_000010.9:g.90963616G= NCBI36
NG_008194.1:g.43025C=

Transcript Alleles

HGVS Amino-acid change
ENST00000336233.10:c.*949C= MANE Select ENSP00000337354.5:n.*949C=
ENST00000336233.9:c.*949C= ENSP00000337354.5:n.*949C=
ENST00000371837.5:c.*949C= ENSP00000360903.1:n.*949C=
ENST00000456827.5:c.*949C= ENSP00000413019.2:n.*949C=
NM_000235.3:c.*949C= NP_000226.2:n.*949C=
NM_001127605.2:c.*949C= NP_001121077.1:n.*949C=
NM_001288979.1:c.*949C= NP_001275908.1:n.*949C=
XM_024448023.1:c.*949C= XP_024303791.1:n.*949C=
NM_000235.4:c.*949C= MANE Select NP_000226.2:n.*949C=
NM_001127605.3:c.*949C= NP_001121077.1:n.*949C=
NM_001288979.2:c.*949C= NP_001275908.1:n.*949C=