Canonical Allele Identifier: CA470737918
Community Standard Title: NM_000235.4(LIPA):c.600G>A (p.Leu200=)
Gene: LIPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89225167C>T , CM000672.2:g.89225167C>T GRCh38
NC_000010.10:g.90984924C>T , CM000672.1:g.90984924C>T GRCh37
NC_000010.9:g.90974904C>T NCBI36
NG_008194.1:g.31737G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000235.4:c.600G>A MANE Select NP_000226.2:p.Leu200=
ENST00000336233.10:c.600G>A MANE Select ENSP00000337354.5:p.Leu200=
NM_000235.3:c.600G>A NP_000226.2:p.Leu200=
NM_001127605.2:c.600G>A NP_001121077.1:p.Leu200=
NM_001127605.3:c.600G>A NP_001121077.1:p.Leu200=
NM_001288979.1:c.252G>A NP_001275908.1:p.Leu84=
NM_001288979.2:c.252G>A NP_001275908.1:p.Leu84=
ENST00000282673.5:c.600G>A ENSP00000282673.4:p.Leu200=
ENST00000336233.9:c.600G>A ENSP00000337354.5:p.Leu200=
ENST00000371837.5:c.432G>A ENSP00000360903.1:p.Leu144=
ENST00000428800.5:c.600G>A ENSP00000388415.1:p.Leu200=
ENST00000456827.5:c.252G>A ENSP00000413019.2:p.Leu84=
XM_024448023.1:c.600G>A XP_024303791.1:p.Leu200=