Canonical Allele Identifier: CA580502380

Gene: LPL

Linked Data

• dbSNP Id: rs1162453137
• gnomAD v2: 8-19809243-G-A
• gnomAD v4: 8-19951732-G-A
• MyVariant Identifiers: chr8:g.19809243G>A (hg19) ; chr8:g.19951732G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951732G>A , CM000670.2:g.19951732G>A	GRCh38
NC_000008.10:g.19809243G>A , CM000670.1:g.19809243G>A	GRCh37
NC_000008.9:g.19853523G>A	NCBI36
NG_008855.1:g.17662G>A
NG_008855.2:g.55016G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.250-37G>A MANE Select	ENSP00000497642.1:n.250-37G>A
ENST00000311322.8:c.250-37G>A	ENSP00000309757.6:n.250-37G>A
ENST00000520959.5:c.22-37G>A	ENSP00000428496.1:n.22-37G>A
ENST00000521994.1:n.470G>A
ENST00000522701.5:c.250-37G>A	ENSP00000428557.1:n.250-37G>A
ENST00000524029.5:c.250-37G>A	ENSP00000428237.1:n.250-37G>A
NM_000237.2:c.250-37G>A	NP_000228.1:n.250-37G>A
NM_000237.3:c.250-37G>A MANE Select	NP_000228.1:n.250-37G>A