Canonical Allele Identifier: CA370464635

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19796977T>A (hg19) ; chr8:g.19939466T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939466T>A , CM000670.2:g.19939466T>A	GRCh38
NC_000008.10:g.19796977T>A , CM000670.1:g.19796977T>A	GRCh37
NC_000008.9:g.19841257T>A	NCBI36
NG_008855.1:g.5396T>A
NG_008855.2:g.42750T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.26T>A MANE Select	ENSP00000497642.1:p.Leu9Gln
ENST00000311322.8:c.26T>A	ENSP00000309757.6:p.Leu9Gln
ENST00000519773.1:c.26T>A	ENSP00000431028.1:p.Leu9Gln
ENST00000520959.5:c.-140-8714T>A	ENSP00000428496.1:n.-140-8714T>A
ENST00000521994.1:n.211T>A
ENST00000522701.5:c.26T>A	ENSP00000428557.1:p.Leu9Gln
ENST00000523696.1:n.95T>A
ENST00000524029.5:c.26T>A	ENSP00000428237.1:p.Leu9Gln
NM_000237.2:c.26T>A	NP_000228.1:p.Leu9Gln
NM_000237.3:c.26T>A MANE Select	NP_000228.1:p.Leu9Gln