Canonical Allele Identifier: CA173379539
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs192934442
gnomAD v2: 8-19816286-A-G
gnomAD v3: 8-19958775-A-G
gnomAD v4: 8-19958775-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958775A>G , CM000670.2:g.19958775A>G GRCh38
NC_000008.10:g.19816286A>G , CM000670.1:g.19816286A>G GRCh37
NC_000008.9:g.19860566A>G NCBI36
NG_008855.1:g.24705A>G
NG_008855.2:g.62059A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-485A>G MANE Select ENSP00000497642.1:n.1019-485A>G
ENST00000650478.1:c.80-2126A>G ENSP00000497560.1:n.80-2126A>G
ENST00000311322.8:c.1019-485A>G ENSP00000309757.6:n.1019-485A>G
NM_000237.2:c.1019-485A>G NP_000228.1:n.1019-485A>G
NM_000237.3:c.1019-485A>G MANE Select NP_000228.1:n.1019-485A>G