Canonical Allele Identifier: CA2579105698

Gene: LPL

Linked Data

• gnomAD v4: 8-19939349-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939349A>C , CM000670.2:g.19939349A>C	GRCh38
NC_000008.10:g.19796860A>C , CM000670.1:g.19796860A>C	GRCh37
NC_000008.9:g.19841140A>C	NCBI36
NG_008855.1:g.5279A>C
NG_008855.2:g.42633A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-92A>C MANE Select	ENSP00000497642.1:n.-92A>C
ENST00000311322.8:c.-92A>C	ENSP00000309757.6:n.-92A>C
ENST00000519773.1:c.-92A>C	ENSP00000431028.1:n.-92A>C
ENST00000520959.5:c.-140-8831A>C	ENSP00000428496.1:n.-140-8831A>C
ENST00000521994.1:n.94A>C
ENST00000522701.5:c.-92A>C	ENSP00000428557.1:n.-92A>C
ENST00000524029.5:c.-92A>C	ENSP00000428237.1:n.-92A>C
NM_000237.2:c.-92A>C	NP_000228.1:n.-92A>C
NM_000237.3:c.-92A>C MANE Select	NP_000228.1:n.-92A>C