Canonical Allele Identifier: CA2686357464
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19939424-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939424G>T , CM000670.2:g.19939424G>T GRCh38
NC_000008.10:g.19796935G>T , CM000670.1:g.19796935G>T GRCh37
NC_000008.9:g.19841215G>T NCBI36
NG_008855.1:g.5354G>T
NG_008855.2:g.42708G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-17G>T MANE Select ENSP00000497642.1:n.-17G>T
ENST00000311322.8:c.-17G>T ENSP00000309757.6:n.-17G>T
ENST00000519773.1:c.-17G>T ENSP00000431028.1:n.-17G>T
ENST00000520959.5:c.-140-8756G>T ENSP00000428496.1:n.-140-8756G>T
ENST00000521994.1:n.169G>T
ENST00000522701.5:c.-17G>T ENSP00000428557.1:n.-17G>T
ENST00000523696.1:n.53G>T
ENST00000524029.5:c.-17G>T ENSP00000428237.1:n.-17G>T
NM_000237.2:c.-17G>T NP_000228.1:n.-17G>T
NM_000237.3:c.-17G>T MANE Select NP_000228.1:n.-17G>T