Canonical Allele Identifier: CA459678467
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19951807-G-C
MyVariant Identifiers: chr8:g.19809318G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951807G>C , CM000670.2:g.19951807G>C GRCh38
NC_000008.10:g.19809318G>C , CM000670.1:g.19809318G>C GRCh37
NC_000008.9:g.19853598G>C NCBI36
NG_008855.1:g.17737G>C
NG_008855.2:g.55091G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.288G>C MANE Select ENSP00000497642.1:p.Val96=
ENST00000311322.8:c.288G>C ENSP00000309757.6:p.Val96=
ENST00000520959.5:c.60G>C ENSP00000428496.1:p.Val20=
ENST00000521994.1:n.545G>C
ENST00000522701.5:c.288G>C ENSP00000428557.1:p.Val96=
ENST00000524029.5:c.288G>C ENSP00000428237.1:p.Val96=
NM_000237.2:c.288G>C NP_000228.1:p.Val96=
NM_000237.3:c.288G>C MANE Select NP_000228.1:p.Val96=
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