Canonical Allele Identifier: CA1769101790
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954099_19954102delinsCCTG , CM000670.2:g.19954099_19954102delinsCCTG GRCh38
NC_000008.10:g.19811610_19811613delinsCCTG , CM000670.1:g.19811610_19811613delinsCCTG GRCh37
NC_000008.9:g.19855890_19855893delinsCCTG NCBI36
NG_008855.1:g.20029_20032delinsCCTG
NG_008855.2:g.57383_57386delinsCCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-21_542-18delinsCCTG MANE Select ENSP00000497642.1:n.542-21_542-18delinsCC...
ENST00000311322.8:c.542-21_542-18delinsCCTG ENSP00000309757.6:n.542-21_542-18delinsCC...
ENST00000520959.5:c.314-21_314-18delinsCCTG ENSP00000428496.1:n.314-21_314-18delinsCC...
NM_000237.2:c.542-21_542-18delinsCCTG NP_000228.1:n.542-21_542-18delinsCCTG
NM_000237.3:c.542-21_542-18delinsCCTG MANE Select NP_000228.1:n.542-21_542-18delinsCCTG