Canonical Allele Identifier: CA1769116778
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967062A= , CM000670.2:g.19967062A= GRCh38
NC_000008.10:g.19824573A= , CM000670.1:g.19824573A= GRCh37
NC_000008.9:g.19868853A= NCBI36
NG_008855.1:g.32992A=
NG_008855.2:g.70346A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1752A= MANE Select ENSP00000497642.1:n.*1752A=
ENST00000650478.1:c.2120A= ENSP00000497560.1:n.2120A=
ENST00000311322.8:c.*1752A= ENSP00000309757.6:n.*1752A=
NM_000237.2:c.*1752A= NP_000228.1:n.*1752A=
NM_000237.3:c.*1752A= MANE Select NP_000228.1:n.*1752A=