Canonical Allele Identifier: CA370638734

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19818513A>T (hg19) ; chr8:g.19961002A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19961002A>T , CM000670.2:g.19961002A>T	GRCh38
NC_000008.10:g.19818513A>T , CM000670.1:g.19818513A>T	GRCh37
NC_000008.9:g.19862793A>T	NCBI36
NG_008855.1:g.26932A>T
NG_008855.2:g.64286A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1241A>T MANE Select	ENSP00000497642.1:p.Tyr414Phe
ENST00000650478.1:c.181A>T	ENSP00000497560.1:n.181A>T
ENST00000311322.8:c.1241A>T	ENSP00000309757.6:p.Tyr414Phe
NM_000237.2:c.1241A>T	NP_000228.1:p.Tyr414Phe
NM_000237.3:c.1241A>T MANE Select	NP_000228.1:p.Tyr414Phe