Canonical Allele Identifier: CA1769102919
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954350G= , CM000670.2:g.19954350G= GRCh38
NC_000008.10:g.19811861G= , CM000670.1:g.19811861G= GRCh37
NC_000008.9:g.19856141G= NCBI36
NG_008855.1:g.20280G=
NG_008855.2:g.57634G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.772G= MANE Select ENSP00000497642.1:p.Gly258=
ENST00000311322.8:c.772G= ENSP00000309757.6:p.Gly258=
NM_000237.2:c.772G= NP_000228.1:p.Gly258=
NM_000237.3:c.772G= MANE Select NP_000228.1:p.Gly258=
Search 100 bp 5'
Search 100 bp 3'