Canonical Allele Identifier: CA2553226881
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954621_19954623del , CM000670.2:g.19954621_19954623del GRCh38
NC_000008.10:g.19812132_19812134del , CM000670.1:g.19812132_19812134del GRCh37
NC_000008.9:g.19856412_19856414del NCBI36
NG_008855.1:g.20551_20553del
NG_008855.2:g.57905_57907del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+268_775+270del MANE Select ENSP00000497642.1:n.775+268_775+270del
ENST00000311322.8:c.775+268_775+270del ENSP00000309757.6:n.775+268_775+270del
NM_000237.2:c.775+268_775+270del NP_000228.1:n.775+268_775+270del
NM_000237.3:c.775+268_775+270del MANE Select NP_000228.1:n.775+268_775+270del