Canonical Allele Identifier: CA1111551601
Gene: LPL HGNC NCBI

Linked Data

gnomAD v3: 8-19954022-A-G
gnomAD v4: 8-19954022-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954022A>G , CM000670.2:g.19954022A>G GRCh38
NC_000008.10:g.19811533A>G , CM000670.1:g.19811533A>G GRCh37
NC_000008.9:g.19855813A>G NCBI36
NG_008855.1:g.19952A>G
NG_008855.2:g.57306A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-98A>G MANE Select ENSP00000497642.1:n.542-98A>G
ENST00000311322.8:c.542-98A>G ENSP00000309757.6:n.542-98A>G
ENST00000520959.5:c.314-98A>G ENSP00000428496.1:n.314-98A>G
NM_000237.2:c.542-98A>G NP_000228.1:n.542-98A>G
NM_000237.3:c.542-98A>G MANE Select NP_000228.1:n.542-98A>G
Search 100 bp 5'
Search 100 bp 3'