Canonical Allele Identifier: CA1926729594

Gene: LIPA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89214193A= , CM000672.2:g.89214193A=	GRCh38
NC_000010.10:g.90973950A= , CM000672.1:g.90973950A=	GRCh37
NC_000010.9:g.90963930A=	NCBI36
NG_008194.1:g.42711T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.*635T= MANE Select	ENSP00000337354.5:n.*635T=
ENST00000336233.9:c.*635T=	ENSP00000337354.5:n.*635T=
ENST00000371837.5:c.*635T=	ENSP00000360903.1:n.*635T=
ENST00000456827.5:c.*635T=	ENSP00000413019.2:n.*635T=
NM_000235.3:c.*635T=	NP_000226.2:n.*635T=
NM_001127605.2:c.*635T=	NP_001121077.1:n.*635T=
NM_001288979.1:c.*635T=	NP_001275908.1:n.*635T=
XM_024448023.1:c.*635T=	XP_024303791.1:n.*635T=
NM_000235.4:c.*635T= MANE Select	NP_000226.2:n.*635T=
NM_001127605.3:c.*635T=	NP_001121077.1:n.*635T=
NM_001288979.2:c.*635T=	NP_001275908.1:n.*635T=