Canonical Allele Identifier: CA459879697

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19813515G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19956004G>T , CM000670.2:g.19956004G>T	GRCh38
NC_000008.10:g.19813515G>T , CM000670.1:g.19813515G>T	GRCh37
NC_000008.9:g.19857795G>T	NCBI36
NG_008855.1:g.21934G>T
NG_008855.2:g.59288G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.939G>T MANE Select	ENSP00000497642.1:p.Leu313=
ENST00000311322.8:c.939G>T	ENSP00000309757.6:p.Leu313=
NM_000237.2:c.939G>T	NP_000228.1:p.Leu313=
NM_000237.3:c.939G>T MANE Select	NP_000228.1:p.Leu313=