Canonical Allele Identifier: CA849565365

Gene: LPL

Linked Data

• dbSNP Id: rs1438966795
• MyVariant Identifiers: chr8:g.19820298C>T (hg19) ; chr8:g.19962787C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19962787C>T , CM000670.2:g.19962787C>T	GRCh38
NC_000008.10:g.19820298C>T , CM000670.1:g.19820298C>T	GRCh37
NC_000008.9:g.19864578C>T	NCBI36
NG_008855.1:g.28717C>T
NG_008855.2:g.66071C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1427+568C>T MANE Select	ENSP00000497642.1:n.1427+568C>T
ENST00000650478.1:c.367+568C>T	ENSP00000497560.1:n.367+568C>T
ENST00000311322.8:c.1427+568C>T	ENSP00000309757.6:n.1427+568C>T
NM_000237.2:c.1427+568C>T	NP_000228.1:n.1427+568C>T
NM_000237.3:c.1427+568C>T MANE Select	NP_000228.1:n.1427+568C>T