Canonical Allele Identifier: CA459879311
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811647A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954136A>C , CM000670.2:g.19954136A>C GRCh38
NC_000008.10:g.19811647A>C , CM000670.1:g.19811647A>C GRCh37
NC_000008.9:g.19855927A>C NCBI36
NG_008855.1:g.20066A>C
NG_008855.2:g.57420A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.558A>C MANE Select ENSP00000497642.1:p.Gly186=
ENST00000311322.8:c.558A>C ENSP00000309757.6:p.Gly186=
ENST00000520959.5:c.330A>C ENSP00000428496.1:p.Gly110=
NM_000237.2:c.558A>C NP_000228.1:p.Gly186=
NM_000237.3:c.558A>C MANE Select NP_000228.1:p.Gly186=