Canonical Allele Identifier: CA1769101578
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953970_19953974delinsGTCTC , CM000670.2:g.19953970_19953974delinsGTCTC GRCh38
NC_000008.10:g.19811481_19811485delinsGTCTC , CM000670.1:g.19811481_19811485delinsGTCTC GRCh37
NC_000008.9:g.19855761_19855765delinsGTCTC NCBI36
NG_008855.1:g.19900_19904delinsGTCTC
NG_008855.2:g.57254_57258delinsGTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-150_542-146delinsGTCTC MANE Select ENSP00000497642.1:n.542-150_542-146delinsGTCTC
ENST00000311322.8:c.542-150_542-146delinsGTCTC ENSP00000309757.6:n.542-150_542-146delinsGTCTC
ENST00000520959.5:c.314-150_314-146delinsGTCTC ENSP00000428496.1:n.314-150_314-146delinsGTCTC
NM_000237.2:c.542-150_542-146delinsGTCTC NP_000228.1:n.542-150_542-146delinsGTCTC
NM_000237.3:c.542-150_542-146delinsGTCTC MANE Select NP_000228.1:n.542-150_542-146delinsGTCTC