Canonical Allele Identifier: CA173618747

Gene: LPL

Linked Data

• dbSNP Id: rs763035747
• MyVariant Identifiers: chr8:g.19824378C>T (hg19) ; chr8:g.19966867C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19966867C>T , CM000670.2:g.19966867C>T	GRCh38
NC_000008.10:g.19824378C>T , CM000670.1:g.19824378C>T	GRCh37
NC_000008.9:g.19868658C>T	NCBI36
NG_008855.1:g.32797C>T
NG_008855.2:g.70151C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.*1557C>T MANE Select	ENSP00000497642.1:n.*1557C>T
ENST00000650478.1:c.1925C>T	ENSP00000497560.1:n.1925C>T
ENST00000311322.8:c.*1557C>T	ENSP00000309757.6:n.*1557C>T
NM_000237.2:c.*1557C>T	NP_000228.1:n.*1557C>T
NM_000237.3:c.*1557C>T MANE Select	NP_000228.1:n.*1557C>T