Canonical Allele Identifier: CA173370962
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs886062787
gnomAD v2: 8-19796914-C-T
gnomAD v3: 8-19939403-C-T
gnomAD v4: 8-19939403-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939403C>T , CM000670.2:g.19939403C>T GRCh38
NC_000008.10:g.19796914C>T , CM000670.1:g.19796914C>T GRCh37
NC_000008.9:g.19841194C>T NCBI36
NG_008855.1:g.5333C>T
NG_008855.2:g.42687C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-38C>T MANE Select ENSP00000497642.1:n.-38C>T
ENST00000311322.8:c.-38C>T ENSP00000309757.6:n.-38C>T
ENST00000519773.1:c.-38C>T ENSP00000431028.1:n.-38C>T
ENST00000520959.5:c.-140-8777C>T ENSP00000428496.1:n.-140-8777C>T
ENST00000521994.1:n.148C>T
ENST00000522701.5:c.-38C>T ENSP00000428557.1:n.-38C>T
ENST00000523696.1:n.32C>T
ENST00000524029.5:c.-38C>T ENSP00000428237.1:n.-38C>T
NM_000237.2:c.-38C>T NP_000228.1:n.-38C>T
NM_000237.3:c.-38C>T MANE Select NP_000228.1:n.-38C>T