Canonical Allele Identifier: CA2686360621

Gene: LPL

Linked Data

• gnomAD v4: 8-19955835-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19955835A>T , CM000670.2:g.19955835A>T	GRCh38
NC_000008.10:g.19813346A>T , CM000670.1:g.19813346A>T	GRCh37
NC_000008.9:g.19857626A>T	NCBI36
NG_008855.1:g.21765A>T
NG_008855.2:g.59119A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.776-6A>T MANE Select	ENSP00000497642.1:n.776-6A>T
ENST00000311322.8:c.776-6A>T	ENSP00000309757.6:n.776-6A>T
NM_000237.2:c.776-6A>T	NP_000228.1:n.776-6A>T
NM_000237.3:c.776-6A>T MANE Select	NP_000228.1:n.776-6A>T