Canonical Allele Identifier: CA370638526

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19818414C>T (hg19) ; chr8:g.19960903C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960903C>T , CM000670.2:g.19960903C>T	GRCh38
NC_000008.10:g.19818414C>T , CM000670.1:g.19818414C>T	GRCh37
NC_000008.9:g.19862694C>T	NCBI36
NG_008855.1:g.26833C>T
NG_008855.2:g.64187C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1142C>T MANE Select	ENSP00000497642.1:p.Pro381Leu
ENST00000650478.1:c.82C>T	ENSP00000497560.1:p.Leu28=
ENST00000311322.8:c.1142C>T	ENSP00000309757.6:p.Pro381Leu
NM_000237.2:c.1142C>T	NP_000228.1:p.Pro381Leu
NM_000237.3:c.1142C>T MANE Select	NP_000228.1:p.Pro381Leu