Canonical Allele Identifier: CA459678483
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19951831-A-G
MyVariant Identifiers: chr8:g.19809342A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951831A>G , CM000670.2:g.19951831A>G GRCh38
NC_000008.10:g.19809342A>G , CM000670.1:g.19809342A>G GRCh37
NC_000008.9:g.19853622A>G NCBI36
NG_008855.1:g.17761A>G
NG_008855.2:g.55115A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.312A>G MANE Select ENSP00000497642.1:p.Pro104=
ENST00000311322.8:c.312A>G ENSP00000309757.6:p.Pro104=
ENST00000520959.5:c.84A>G ENSP00000428496.1:p.Pro28=
ENST00000522701.5:c.312A>G ENSP00000428557.1:p.Pro104=
ENST00000524029.5:c.312A>G ENSP00000428237.1:p.Pro104=
NM_000237.2:c.312A>G NP_000228.1:p.Pro104=
NM_000237.3:c.312A>G MANE Select NP_000228.1:p.Pro104=