Canonical Allele Identifier: CA1769106767
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957680G= , CM000670.2:g.19957680G= GRCh38
NC_000008.10:g.19815191G= , CM000670.1:g.19815191G= GRCh37
NC_000008.9:g.19859471G= NCBI36
NG_008855.1:g.23610G=
NG_008855.2:g.60964G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1580G= MANE Select ENSP00000497642.1:n.1019-1580G=
ENST00000650478.1:c.79+1597G= ENSP00000497560.1:n.79+1597G=
ENST00000311322.8:c.1019-1580G= ENSP00000309757.6:n.1019-1580G=
NM_000237.2:c.1019-1580G= NP_000228.1:n.1019-1580G=
NM_000237.3:c.1019-1580G= MANE Select NP_000228.1:n.1019-1580G=