Canonical Allele Identifier: CA1769116961
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967204C= , CM000670.2:g.19967204C= GRCh38
NC_000008.10:g.19824715C= , CM000670.1:g.19824715C= GRCh37
NC_000008.9:g.19868995C= NCBI36
NG_008855.1:g.33134C=
NG_008855.2:g.70488C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1894C= MANE Select ENSP00000497642.1:n.*1894C=
ENST00000311322.8:c.*1894C= ENSP00000309757.6:n.*1894C=
NM_000237.2:c.*1894C= NP_000228.1:n.*1894C=
NM_000237.3:c.*1894C= MANE Select NP_000228.1:n.*1894C=