Canonical Allele Identifier: CA1769116520
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966779T= , CM000670.2:g.19966779T= GRCh38
NC_000008.10:g.19824290T= , CM000670.1:g.19824290T= GRCh37
NC_000008.9:g.19868570T= NCBI36
NG_008855.1:g.32709T=
NG_008855.2:g.70063T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1469T= MANE Select ENSP00000497642.1:n.*1469T=
ENST00000650478.1:c.1837T= ENSP00000497560.1:n.1837T=
ENST00000311322.8:c.*1469T= ENSP00000309757.6:n.*1469T=
NM_000237.2:c.*1469T= NP_000228.1:n.*1469T=
NM_000237.3:c.*1469T= MANE Select NP_000228.1:n.*1469T=