Canonical Allele Identifier: CA849549607

Gene: LPL

Linked Data

• dbSNP Id: rs1253033219
• gnomAD v3: 8-19939289-G-T
• gnomAD v4: 8-19939289-G-T
• MyVariant Identifiers: chr8:g.19796800G>T (hg19) ; chr8:g.19939289G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939289G>T , CM000670.2:g.19939289G>T	GRCh38
NC_000008.10:g.19796800G>T , CM000670.1:g.19796800G>T	GRCh37
NC_000008.9:g.19841080G>T	NCBI36
NG_008855.1:g.5219G>T
NG_008855.2:g.42573G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-152G>T MANE Select	ENSP00000497642.1:n.-152G>T
ENST00000311322.8:c.-152G>T	ENSP00000309757.6:n.-152G>T
ENST00000519773.1:c.-152G>T	ENSP00000431028.1:n.-152G>T
ENST00000520959.5:c.-140-8891G>T	ENSP00000428496.1:n.-140-8891G>T
ENST00000521994.1:n.34G>T
ENST00000522701.5:c.-152G>T	ENSP00000428557.1:n.-152G>T
ENST00000524029.5:c.-152G>T	ENSP00000428237.1:n.-152G>T
NM_000237.2:c.-152G>T	NP_000228.1:n.-152G>T
NM_000237.3:c.-152G>T MANE Select	NP_000228.1:n.-152G>T