Canonical Allele Identifier: CA849568013

Gene: LPL

Linked Data

• dbSNP Id: rs13702
• MyVariant Identifiers: chr8:g.19824492T>A (hg19) ; chr8:g.19966981T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19966981T>A , CM000670.2:g.19966981T>A	GRCh38
NC_000008.10:g.19824492T>A , CM000670.1:g.19824492T>A	GRCh37
NC_000008.9:g.19868772T>A	NCBI36
NG_008855.1:g.32911T>A
NG_008855.2:g.70265T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.*1671T>A MANE Select	ENSP00000497642.1:n.*1671T>A
ENST00000650478.1:c.2039T>A	ENSP00000497560.1:n.2039T>A
ENST00000311322.8:c.*1671T>A	ENSP00000309757.6:n.*1671T>A
NM_000237.2:c.*1671T>A	NP_000228.1:n.*1671T>A
NM_000237.3:c.*1671T>A MANE Select	NP_000228.1:n.*1671T>A