Canonical Allele Identifier: CA377517775

Gene: LIPA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89228222G>A , CM000672.2:g.89228222G>A	GRCh38
NC_000010.10:g.90987979G>A , CM000672.1:g.90987979G>A	GRCh37
NC_000010.9:g.90977959G>A	NCBI36
NG_008194.1:g.28682C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000235.4:c.406C>T MANE Select	NP_000226.2:p.Gln136Ter
ENST00000336233.10:c.406C>T MANE Select	ENSP00000337354.5:p.Gln136Ter
NM_000235.3:c.406C>T	NP_000226.2:p.Gln136Ter
NM_001127605.2:c.406C>T	NP_001121077.1:p.Gln136Ter
NM_001127605.3:c.406C>T	NP_001121077.1:p.Gln136Ter
NM_001288979.1:c.58C>T	NP_001275908.1:p.Gln20Ter
NM_001288979.2:c.58C>T	NP_001275908.1:p.Gln20Ter
ENST00000282673.5:c.406C>T	ENSP00000282673.4:p.Gln136Ter
ENST00000336233.9:c.406C>T	ENSP00000337354.5:p.Gln136Ter
ENST00000371837.5:c.238C>T	ENSP00000360903.1:p.Gln80Ter
ENST00000428800.5:c.406C>T	ENSP00000388415.1:p.Gln136Ter
ENST00000456827.5:c.58C>T	ENSP00000413019.2:p.Gln20Ter
XM_024448023.1:c.406C>T	XP_024303791.1:p.Gln136Ter