Canonical Allele Identifier: CA4655240
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs535892656
gnomAD v2: 8-19796905-T-G
gnomAD v3: 8-19939394-T-G
gnomAD v4: 8-19939394-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939394T>G , CM000670.2:g.19939394T>G GRCh38
NC_000008.10:g.19796905T>G , CM000670.1:g.19796905T>G GRCh37
NC_000008.9:g.19841185T>G NCBI36
NG_008855.1:g.5324T>G
NG_008855.2:g.42678T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-47T>G MANE Select ENSP00000497642.1:n.-47T>G
ENST00000311322.8:c.-47T>G ENSP00000309757.6:n.-47T>G
ENST00000519773.1:c.-47T>G ENSP00000431028.1:n.-47T>G
ENST00000520959.5:c.-140-8786T>G ENSP00000428496.1:n.-140-8786T>G
ENST00000521994.1:n.139T>G
ENST00000522701.5:c.-47T>G ENSP00000428557.1:n.-47T>G
ENST00000523696.1:n.23T>G
ENST00000524029.5:c.-47T>G ENSP00000428237.1:n.-47T>G
NM_000237.2:c.-47T>G NP_000228.1:n.-47T>G
NM_000237.3:c.-47T>G MANE Select NP_000228.1:n.-47T>G