Canonical Allele Identifier: CA1769097150
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951593G= , CM000670.2:g.19951593G= GRCh38
NC_000008.10:g.19809104G= , CM000670.1:g.19809104G= GRCh37
NC_000008.9:g.19853384G= NCBI36
NG_008855.1:g.17523G=
NG_008855.2:g.54877G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-176G= MANE Select ENSP00000497642.1:n.250-176G=
ENST00000311322.8:c.250-176G= ENSP00000309757.6:n.250-176G=
ENST00000520959.5:c.22-176G= ENSP00000428496.1:n.22-176G=
ENST00000521994.1:n.435-104G=
ENST00000522701.5:c.250-176G= ENSP00000428557.1:n.250-176G=
ENST00000524029.5:c.250-176G= ENSP00000428237.1:n.250-176G=
NM_000237.2:c.250-176G= NP_000228.1:n.250-176G=
NM_000237.3:c.250-176G= MANE Select NP_000228.1:n.250-176G=