Canonical Allele Identifier: CA849562277

Gene: LPL

Linked Data

• dbSNP Id: rs1440545248
• MyVariant Identifiers: chr8:g.19816278A>C (hg19) ; chr8:g.19958767A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19958767A>C , CM000670.2:g.19958767A>C	GRCh38
NC_000008.10:g.19816278A>C , CM000670.1:g.19816278A>C	GRCh37
NC_000008.9:g.19860558A>C	NCBI36
NG_008855.1:g.24697A>C
NG_008855.2:g.62051A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.1019-493A>C MANE Select	ENSP00000497642.1:n.1019-493A>C
ENST00000650478.1:c.80-2134A>C	ENSP00000497560.1:n.80-2134A>C
ENST00000311322.8:c.1019-493A>C	ENSP00000309757.6:n.1019-493A>C
NM_000237.2:c.1019-493A>C	NP_000228.1:n.1019-493A>C
NM_000237.3:c.1019-493A>C MANE Select	NP_000228.1:n.1019-493A>C