Canonical Allele Identifier: CA1769116755
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070095734

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967045G>A , CM000670.2:g.19967045G>A GRCh38
NC_000008.10:g.19824556G>A , CM000670.1:g.19824556G>A GRCh37
NC_000008.9:g.19868836G>A NCBI36
NG_008855.1:g.32975G>A
NG_008855.2:g.70329G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1735G>A MANE Select ENSP00000497642.1:n.*1735G>A
ENST00000650478.1:c.2103G>A ENSP00000497560.1:n.2103G>A
ENST00000311322.8:c.*1735G>A ENSP00000309757.6:n.*1735G>A
NM_000237.2:c.*1735G>A NP_000228.1:n.*1735G>A
NM_000237.3:c.*1735G>A MANE Select NP_000228.1:n.*1735G>A