Canonical Allele Identifier: CA370469299

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19813520A>C (hg19) ; chr8:g.19956009A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19956009A>C , CM000670.2:g.19956009A>C	GRCh38
NC_000008.10:g.19813520A>C , CM000670.1:g.19813520A>C	GRCh37
NC_000008.9:g.19857800A>C	NCBI36
NG_008855.1:g.21939A>C
NG_008855.2:g.59293A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.944A>C MANE Select	ENSP00000497642.1:p.Tyr315Ser
ENST00000650478.1:c.5A>C	ENSP00000497560.1:p.Tyr2Ser
ENST00000311322.8:c.944A>C	ENSP00000309757.6:p.Tyr315Ser
NM_000237.2:c.944A>C	NP_000228.1:p.Tyr315Ser
NM_000237.3:c.944A>C MANE Select	NP_000228.1:p.Tyr315Ser