Canonical Allele Identifier: CA370467350

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809293A>C (hg19) ; chr8:g.19951782A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951782A>C , CM000670.2:g.19951782A>C	GRCh38
NC_000008.10:g.19809293A>C , CM000670.1:g.19809293A>C	GRCh37
NC_000008.9:g.19853573A>C	NCBI36
NG_008855.1:g.17712A>C
NG_008855.2:g.55066A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.263A>C MANE Select	ENSP00000497642.1:p.Tyr88Ser
ENST00000311322.8:c.263A>C	ENSP00000309757.6:p.Tyr88Ser
ENST00000520959.5:c.35A>C	ENSP00000428496.1:p.Tyr12Ser
ENST00000521994.1:n.520A>C
ENST00000522701.5:c.263A>C	ENSP00000428557.1:p.Tyr88Ser
ENST00000524029.5:c.263A>C	ENSP00000428237.1:p.Tyr88Ser
NM_000237.2:c.263A>C	NP_000228.1:p.Tyr88Ser
NM_000237.3:c.263A>C MANE Select	NP_000228.1:p.Tyr88Ser