Canonical Allele Identifier: CA1769116594
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966851A= , CM000670.2:g.19966851A= GRCh38
NC_000008.10:g.19824362A= , CM000670.1:g.19824362A= GRCh37
NC_000008.9:g.19868642A= NCBI36
NG_008855.1:g.32781A=
NG_008855.2:g.70135A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1541A= MANE Select ENSP00000497642.1:n.*1541A=
ENST00000650478.1:c.1909A= ENSP00000497560.1:n.1909A=
ENST00000311322.8:c.*1541A= ENSP00000309757.6:n.*1541A=
NM_000237.2:c.*1541A= NP_000228.1:n.*1541A=
NM_000237.3:c.*1541A= MANE Select NP_000228.1:n.*1541A=