Canonical Allele Identifier: CA370638568

Gene: LPL

Linked Data

• gnomAD v4: 8-19960923-A-T
• MyVariant Identifiers: chr8:g.19818434A>T (hg19) ; chr8:g.19960923A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960923A>T , CM000670.2:g.19960923A>T	GRCh38
NC_000008.10:g.19818434A>T , CM000670.1:g.19818434A>T	GRCh37
NC_000008.9:g.19862714A>T	NCBI36
NG_008855.1:g.26853A>T
NG_008855.2:g.64207A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.1162A>T MANE Select	ENSP00000497642.1:p.Thr388Ser
ENST00000650478.1:c.102A>T	ENSP00000497560.1:p.Arg34Ser
ENST00000311322.8:c.1162A>T	ENSP00000309757.6:p.Thr388Ser
NM_000237.2:c.1162A>T	NP_000228.1:p.Thr388Ser
NM_000237.3:c.1162A>T MANE Select	NP_000228.1:p.Thr388Ser