Canonical Allele Identifier: CA580209976
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1191177716
gnomAD v2: 8-19824516-C-G
gnomAD v3: 8-19967005-C-G
gnomAD v4: 8-19967005-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967005C>G , CM000670.2:g.19967005C>G GRCh38
NC_000008.10:g.19824516C>G , CM000670.1:g.19824516C>G GRCh37
NC_000008.9:g.19868796C>G NCBI36
NG_008855.1:g.32935C>G
NG_008855.2:g.70289C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1695C>G MANE Select ENSP00000497642.1:n.*1695C>G
ENST00000650478.1:c.2063C>G ENSP00000497560.1:n.2063C>G
ENST00000311322.8:c.*1695C>G ENSP00000309757.6:n.*1695C>G
NM_000237.2:c.*1695C>G NP_000228.1:n.*1695C>G
NM_000237.3:c.*1695C>G MANE Select NP_000228.1:n.*1695C>G