Canonical Allele Identifier: CA2521170297
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89213886T>A , CM000672.2:g.89213886T>A GRCh38
NC_000010.10:g.90973643T>A , CM000672.1:g.90973643T>A GRCh37
NC_000010.9:g.90963623T>A NCBI36
NG_008194.1:g.43018A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336233.10:c.*942A>T MANE Select ENSP00000337354.5:n.*942A>T
ENST00000336233.9:c.*942A>T ENSP00000337354.5:n.*942A>T
ENST00000371837.5:c.*942A>T ENSP00000360903.1:n.*942A>T
ENST00000456827.5:c.*942A>T ENSP00000413019.2:n.*942A>T
NM_000235.3:c.*942A>T NP_000226.2:n.*942A>T
NM_001127605.2:c.*942A>T NP_001121077.1:n.*942A>T
NM_001288979.1:c.*942A>T NP_001275908.1:n.*942A>T
XM_024448023.1:c.*942A>T XP_024303791.1:n.*942A>T
NM_000235.4:c.*942A>T MANE Select NP_000226.2:n.*942A>T
NM_001127605.3:c.*942A>T NP_001121077.1:n.*942A>T
NM_001288979.2:c.*942A>T NP_001275908.1:n.*942A>T