Canonical Allele Identifier: CA4655458
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs375347152
gnomAD v2: 8-19811599-A-G
gnomAD v3: 8-19954088-A-G
gnomAD v4: 8-19954088-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954088A>G , CM000670.2:g.19954088A>G GRCh38
NC_000008.10:g.19811599A>G , CM000670.1:g.19811599A>G GRCh37
NC_000008.9:g.19855879A>G NCBI36
NG_008855.1:g.20018A>G
NG_008855.2:g.57372A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-32A>G MANE Select ENSP00000497642.1:n.542-32A>G
ENST00000311322.8:c.542-32A>G ENSP00000309757.6:n.542-32A>G
ENST00000520959.5:c.314-32A>G ENSP00000428496.1:n.314-32A>G
NM_000237.2:c.542-32A>G NP_000228.1:n.542-32A>G
NM_000237.3:c.542-32A>G MANE Select NP_000228.1:n.542-32A>G