Canonical Allele Identifier: CA849549647

Gene: LPL

Linked Data

• dbSNP Id: rs1348786436
• gnomAD v4: 8-19939388-G-C
• MyVariant Identifiers: chr8:g.19796899G>C (hg19) ; chr8:g.19939388G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939388G>C , CM000670.2:g.19939388G>C	GRCh38
NC_000008.10:g.19796899G>C , CM000670.1:g.19796899G>C	GRCh37
NC_000008.9:g.19841179G>C	NCBI36
NG_008855.1:g.5318G>C
NG_008855.2:g.42672G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-53G>C MANE Select	ENSP00000497642.1:n.-53G>C
ENST00000311322.8:c.-53G>C	ENSP00000309757.6:n.-53G>C
ENST00000519773.1:c.-53G>C	ENSP00000431028.1:n.-53G>C
ENST00000520959.5:c.-140-8792G>C	ENSP00000428496.1:n.-140-8792G>C
ENST00000521994.1:n.133G>C
ENST00000522701.5:c.-53G>C	ENSP00000428557.1:n.-53G>C
ENST00000523696.1:n.17G>C
ENST00000524029.5:c.-53G>C	ENSP00000428237.1:n.-53G>C
NM_000237.2:c.-53G>C	NP_000228.1:n.-53G>C
NM_000237.3:c.-53G>C MANE Select	NP_000228.1:n.-53G>C