Canonical Allele Identifier: CA370467638

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809391T>G (hg19) ; chr8:g.19951880T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951880T>G , CM000670.2:g.19951880T>G	GRCh38
NC_000008.10:g.19809391T>G , CM000670.1:g.19809391T>G	GRCh37
NC_000008.9:g.19853671T>G	NCBI36
NG_008855.1:g.17810T>G
NG_008855.2:g.55164T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.361T>G MANE Select	ENSP00000497642.1:p.Tyr121Asp
ENST00000311322.8:c.361T>G	ENSP00000309757.6:p.Tyr121Asp
ENST00000520959.5:c.133T>G	ENSP00000428496.1:p.Tyr45Asp
ENST00000524029.5:c.361T>G	ENSP00000428237.1:p.Tyr121Asp
NM_000237.2:c.361T>G	NP_000228.1:p.Tyr121Asp
NM_000237.3:c.361T>G MANE Select	NP_000228.1:p.Tyr121Asp