Canonical Allele Identifier: CA370638558
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19818431A>C (hg19) chr8:g.19960920A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960920A>C , CM000670.2:g.19960920A>C GRCh38
NC_000008.10:g.19818431A>C , CM000670.1:g.19818431A>C GRCh37
NC_000008.9:g.19862711A>C NCBI36
NG_008855.1:g.26850A>C
NG_008855.2:g.64204A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1159A>C MANE Select ENSP00000497642.1:p.Lys387Gln
ENST00000650478.1:c.99A>C ENSP00000497560.1:p.Ile33=
ENST00000311322.8:c.1159A>C ENSP00000309757.6:p.Lys387Gln
NM_000237.2:c.1159A>C NP_000228.1:p.Lys387Gln
NM_000237.3:c.1159A>C MANE Select NP_000228.1:p.Lys387Gln
Search 100 bp 5'
Search 100 bp 3'