Canonical Allele Identifier: CA459678518
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19951885-A-C
MyVariant Identifiers: chr8:g.19809396A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951885A>C , CM000670.2:g.19951885A>C GRCh38
NC_000008.10:g.19809396A>C , CM000670.1:g.19809396A>C GRCh37
NC_000008.9:g.19853676A>C NCBI36
NG_008855.1:g.17815A>C
NG_008855.2:g.55169A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.366A>C MANE Select ENSP00000497642.1:p.Pro122=
ENST00000311322.8:c.366A>C ENSP00000309757.6:p.Pro122=
ENST00000520959.5:c.138A>C ENSP00000428496.1:p.Pro46=
ENST00000524029.5:c.366A>C ENSP00000428237.1:p.Pro122=
NM_000237.2:c.366A>C NP_000228.1:p.Pro122=
NM_000237.3:c.366A>C MANE Select NP_000228.1:p.Pro122=
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