Canonical Allele Identifier: CA1769101608
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953998T= , CM000670.2:g.19953998T= GRCh38
NC_000008.10:g.19811509T= , CM000670.1:g.19811509T= GRCh37
NC_000008.9:g.19855789T= NCBI36
NG_008855.1:g.19928T=
NG_008855.2:g.57282T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-122T= MANE Select ENSP00000497642.1:n.542-122T=
ENST00000311322.8:c.542-122T= ENSP00000309757.6:n.542-122T=
ENST00000520959.5:c.314-122T= ENSP00000428496.1:n.314-122T=
NM_000237.2:c.542-122T= NP_000228.1:n.542-122T=
NM_000237.3:c.542-122T= MANE Select NP_000228.1:n.542-122T=