Canonical Allele Identifier: CA1769116517
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966777A= , CM000670.2:g.19966777A= GRCh38
NC_000008.10:g.19824288A= , CM000670.1:g.19824288A= GRCh37
NC_000008.9:g.19868568A= NCBI36
NG_008855.1:g.32707A=
NG_008855.2:g.70061A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1467A= MANE Select ENSP00000497642.1:n.*1467A=
ENST00000650478.1:c.1835A= ENSP00000497560.1:n.1835A=
ENST00000311322.8:c.*1467A= ENSP00000309757.6:n.*1467A=
NM_000237.2:c.*1467A= NP_000228.1:n.*1467A=
NM_000237.3:c.*1467A= MANE Select NP_000228.1:n.*1467A=