Canonical Allele Identifier: CA370468941
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813358A>C (hg19) chr8:g.19955847A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955847A>C , CM000670.2:g.19955847A>C GRCh38
NC_000008.10:g.19813358A>C , CM000670.1:g.19813358A>C GRCh37
NC_000008.9:g.19857638A>C NCBI36
NG_008855.1:g.21777A>C
NG_008855.2:g.59131A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.782A>C MANE Select ENSP00000497642.1:p.Asp261Ala
ENST00000311322.8:c.782A>C ENSP00000309757.6:p.Asp261Ala
NM_000237.2:c.782A>C NP_000228.1:p.Asp261Ala
NM_000237.3:c.782A>C MANE Select NP_000228.1:p.Asp261Ala
Search 100 bp 5'
Search 100 bp 3'