Canonical Allele Identifier: CA370469165

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19813460A>C (hg19) ; chr8:g.19955949A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19955949A>C , CM000670.2:g.19955949A>C	GRCh38
NC_000008.10:g.19813460A>C , CM000670.1:g.19813460A>C	GRCh37
NC_000008.9:g.19857740A>C	NCBI36
NG_008855.1:g.21879A>C
NG_008855.2:g.59233A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.884A>C MANE Select	ENSP00000497642.1:p.Glu295Ala
ENST00000311322.8:c.884A>C	ENSP00000309757.6:p.Glu295Ala
NM_000237.2:c.884A>C	NP_000228.1:p.Glu295Ala
NM_000237.3:c.884A>C MANE Select	NP_000228.1:p.Glu295Ala