Canonical Allele Identifier: CA1769111552

Gene: LPL

Linked Data

• dbSNP Id: rs2070040799

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19961707A>T , CM000670.2:g.19961707A>T	GRCh38
NC_000008.10:g.19819218A>T , CM000670.1:g.19819218A>T	GRCh37
NC_000008.9:g.19863498A>T	NCBI36
NG_008855.1:g.27637A>T
NG_008855.2:g.64991A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.1323-408A>T MANE Select	ENSP00000497642.1:n.1323-408A>T
ENST00000650478.1:c.263-408A>T	ENSP00000497560.1:n.263-408A>T
ENST00000311322.8:c.1323-408A>T	ENSP00000309757.6:n.1323-408A>T
NM_000237.2:c.1323-408A>T	NP_000228.1:n.1323-408A>T
NM_000237.3:c.1323-408A>T MANE Select	NP_000228.1:n.1323-408A>T