Canonical Allele Identifier: CA459879714
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813545A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956034A>G , CM000670.2:g.19956034A>G GRCh38
NC_000008.10:g.19813545A>G , CM000670.1:g.19813545A>G GRCh37
NC_000008.9:g.19857825A>G NCBI36
NG_008855.1:g.21964A>G
NG_008855.2:g.59318A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.969A>G MANE Select ENSP00000497642.1:p.Lys323=
ENST00000650478.1:c.30A>G ENSP00000497560.1:p.Lys10=
ENST00000311322.8:c.969A>G ENSP00000309757.6:p.Lys323=
NM_000237.2:c.969A>G NP_000228.1:p.Lys323=
NM_000237.3:c.969A>G MANE Select NP_000228.1:p.Lys323=
Search 100 bp 5'
Search 100 bp 3'