Canonical Allele Identifier: CA1769098479
Gene: LPL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952196G= , CM000670.2:g.19952196G= GRCh38
NC_000008.10:g.19809707G= , CM000670.1:g.19809707G= GRCh37
NC_000008.9:g.19853987G= NCBI36
NG_008855.1:g.18126G=
NG_008855.2:g.55480G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+248G= MANE Select ENSP00000497642.1:n.429+248G=
ENST00000311322.8:c.429+248G= ENSP00000309757.6:n.429+248G=
ENST00000520959.5:c.201+248G= ENSP00000428496.1:n.201+248G=
NM_000237.2:c.429+248G= NP_000228.1:n.429+248G=
NM_000237.3:c.429+248G= MANE Select NP_000228.1:n.429+248G=
Search 100 bp 5'
Search 100 bp 3'