Canonical Allele Identifier: CA580502379

Gene: LPL

Linked Data

• dbSNP Id: rs1460875259
• gnomAD v2: 8-19809239-G-C
• gnomAD v4: 8-19951728-G-C
• MyVariant Identifiers: chr8:g.19809239G>C (hg19) ; chr8:g.19951728G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951728G>C , CM000670.2:g.19951728G>C	GRCh38
NC_000008.10:g.19809239G>C , CM000670.1:g.19809239G>C	GRCh37
NC_000008.9:g.19853519G>C	NCBI36
NG_008855.1:g.17658G>C
NG_008855.2:g.55012G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.250-41G>C MANE Select	ENSP00000497642.1:n.250-41G>C
ENST00000311322.8:c.250-41G>C	ENSP00000309757.6:n.250-41G>C
ENST00000520959.5:c.22-41G>C	ENSP00000428496.1:n.22-41G>C
ENST00000521994.1:n.466G>C
ENST00000522701.5:c.250-41G>C	ENSP00000428557.1:n.250-41G>C
ENST00000524029.5:c.250-41G>C	ENSP00000428237.1:n.250-41G>C
NM_000237.2:c.250-41G>C	NP_000228.1:n.250-41G>C
NM_000237.3:c.250-41G>C MANE Select	NP_000228.1:n.250-41G>C