Canonical Allele Identifier: CA5593712
Community Standard Title: NM_000235.4(LIPA):c.483T>C (p.Asn161=)
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89226950A>G , CM000672.2:g.89226950A>G GRCh38
NC_000010.10:g.90986707A>G , CM000672.1:g.90986707A>G GRCh37
NC_000010.9:g.90976687A>G NCBI36
NG_008194.1:g.29954T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000235.4:c.483T>C MANE Select NP_000226.2:p.Asn161=
ENST00000336233.10:c.483T>C MANE Select ENSP00000337354.5:p.Asn161=
NM_000235.3:c.483T>C NP_000226.2:p.Asn161=
NM_001127605.2:c.483T>C NP_001121077.1:p.Asn161=
NM_001127605.3:c.483T>C NP_001121077.1:p.Asn161=
NM_001288979.1:c.135T>C NP_001275908.1:p.Asn45=
NM_001288979.2:c.135T>C NP_001275908.1:p.Asn45=
ENST00000282673.5:c.483T>C ENSP00000282673.4:p.Asn161=
ENST00000336233.9:c.483T>C ENSP00000337354.5:p.Asn161=
ENST00000371837.5:c.315T>C ENSP00000360903.1:p.Asn105=
ENST00000428800.5:c.483T>C ENSP00000388415.1:p.Asn161=
ENST00000456827.5:c.135T>C ENSP00000413019.2:p.Asn45=
XM_024448023.1:c.483T>C XP_024303791.1:p.Asn161=