Canonical Allele Identifier: CA652181312
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070002884
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958036T>A , CM000670.2:g.19958036T>A GRCh38
NC_000008.10:g.19815547T>A , CM000670.1:g.19815547T>A GRCh37
NC_000008.9:g.19859827T>A NCBI36
NG_008855.1:g.23966T>A
NG_008855.2:g.61320T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1224T>A MANE Select ENSP00000497642.1:n.1019-1224T>A
ENST00000650478.1:c.79+1953T>A ENSP00000497560.1:n.79+1953T>A
ENST00000311322.8:c.1019-1224T>A ENSP00000309757.6:n.1019-1224T>A
NM_000237.2:c.1019-1224T>A NP_000228.1:n.1019-1224T>A
NM_000237.3:c.1019-1224T>A MANE Select NP_000228.1:n.1019-1224T>A
Search 100 bp 5'
Search 100 bp 3'