Canonical Allele Identifier: CA2686364561

Gene: LPL

Linked Data

• gnomAD v4: 8-19966732-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19966732G>T , CM000670.2:g.19966732G>T	GRCh38
NC_000008.10:g.19824243G>T , CM000670.1:g.19824243G>T	GRCh37
NC_000008.9:g.19868523G>T	NCBI36
NG_008855.1:g.32662G>T
NG_008855.2:g.70016G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.*1422G>T MANE Select	ENSP00000497642.1:n.*1422G>T
ENST00000650478.1:c.1790G>T	ENSP00000497560.1:n.1790G>T
ENST00000311322.8:c.*1422G>T	ENSP00000309757.6:n.*1422G>T
NM_000237.2:c.*1422G>T	NP_000228.1:n.*1422G>T
NM_000237.3:c.*1422G>T MANE Select	NP_000228.1:n.*1422G>T