Canonical Allele Identifier: CA2686360444
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19954106-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954106T>G , CM000670.2:g.19954106T>G GRCh38
NC_000008.10:g.19811617T>G , CM000670.1:g.19811617T>G GRCh37
NC_000008.9:g.19855897T>G NCBI36
NG_008855.1:g.20036T>G
NG_008855.2:g.57390T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-14T>G MANE Select ENSP00000497642.1:n.542-14T>G
ENST00000311322.8:c.542-14T>G ENSP00000309757.6:n.542-14T>G
ENST00000520959.5:c.314-14T>G ENSP00000428496.1:n.314-14T>G
NM_000237.2:c.542-14T>G NP_000228.1:n.542-14T>G
NM_000237.3:c.542-14T>G MANE Select NP_000228.1:n.542-14T>G