Canonical Allele Identifier: CA849558860
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1395531746
gnomAD v3: 8-19954060-T-G
gnomAD v4: 8-19954060-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954060T>G , CM000670.2:g.19954060T>G GRCh38
NC_000008.10:g.19811571T>G , CM000670.1:g.19811571T>G GRCh37
NC_000008.9:g.19855851T>G NCBI36
NG_008855.1:g.19990T>G
NG_008855.2:g.57344T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-60T>G MANE Select ENSP00000497642.1:n.542-60T>G
ENST00000311322.8:c.542-60T>G ENSP00000309757.6:n.542-60T>G
ENST00000520959.5:c.314-60T>G ENSP00000428496.1:n.314-60T>G
NM_000237.2:c.542-60T>G NP_000228.1:n.542-60T>G
NM_000237.3:c.542-60T>G MANE Select NP_000228.1:n.542-60T>G