Canonical Allele Identifier: CA2686361985

Gene: LPL

Linked Data

• gnomAD v4: 8-19961990-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19961990G>T , CM000670.2:g.19961990G>T	GRCh38
NC_000008.10:g.19819501G>T , CM000670.1:g.19819501G>T	GRCh37
NC_000008.9:g.19863781G>T	NCBI36
NG_008855.1:g.27920G>T
NG_008855.2:g.65274G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1323-125G>T MANE Select	ENSP00000497642.1:n.1323-125G>T
ENST00000650478.1:c.263-125G>T	ENSP00000497560.1:n.263-125G>T
ENST00000311322.8:c.1323-125G>T	ENSP00000309757.6:n.1323-125G>T
NM_000237.2:c.1323-125G>T	NP_000228.1:n.1323-125G>T
NM_000237.3:c.1323-125G>T MANE Select	NP_000228.1:n.1323-125G>T