Canonical Allele Identifier: CA2610081908

Gene: LIPA

Linked Data

• gnomAD v4: 10-89247409-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89247409_89247410insTT , CM000672.2:g.89247409_89247410insTT	GRCh38
NC_000010.10:g.91007166_91007167insTT , CM000672.1:g.91007166_91007167insTT	GRCh37
NC_000010.9:g.90997146_90997147insTT	NCBI36
NG_008194.1:g.9494_9495insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336233.10:c.111+128_111+129insAA MANE Select	ENSP00000337354.5:n.111+128_111+129insAA
ENST00000282673.5:c.111+128_111+129insAA	ENSP00000282673.4:n.111+128_111+129insAA
ENST00000336233.9:c.111+128_111+129insAA	ENSP00000337354.5:n.111+128_111+129insAA
ENST00000371837.5:c.62-19012_62-19011insAA	ENSP00000360903.1:n.62-19012_62-19011insAA
ENST00000428800.5:c.111+128_111+129insAA	ENSP00000388415.1:n.111+128_111+129insAA
ENST00000456827.5:c.-120+4327_-120+4328insAA	ENSP00000413019.2:n.-120+4327_-120+4328insAA
NM_000235.3:c.111+128_111+129insAA	NP_000226.2:n.111+128_111+129insAA
NM_001127605.2:c.111+128_111+129insAA	NP_001121077.1:n.111+128_111+129insAA
NM_001288979.1:c.-120+4327_-120+4328insAA	NP_001275908.1:n.-120+4327_-120+4328insAA
XM_024448023.1:c.111+128_111+129insAA	XP_024303791.1:n.111+128_111+129insAA
NM_000235.4:c.111+128_111+129insAA MANE Select	NP_000226.2:n.111+128_111+129insAA
NM_001127605.3:c.111+128_111+129insAA	NP_001121077.1:n.111+128_111+129insAA
NM_001288979.2:c.-120+4327_-120+4328insAA	NP_001275908.1:n.-120+4327_-120+4328insAA