Canonical Allele Identifier: CA1769112621

Gene: LPL

Linked Data

• dbSNP Id: rs2070052117

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19962881G>T , CM000670.2:g.19962881G>T	GRCh38
NC_000008.10:g.19820392G>T , CM000670.1:g.19820392G>T	GRCh37
NC_000008.9:g.19864672G>T	NCBI36
NG_008855.1:g.28811G>T
NG_008855.2:g.66165G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1427+662G>T MANE Select	ENSP00000497642.1:n.1427+662G>T
ENST00000650478.1:c.367+662G>T	ENSP00000497560.1:n.367+662G>T
ENST00000311322.8:c.1427+662G>T	ENSP00000309757.6:n.1427+662G>T
NM_000237.2:c.1427+662G>T	NP_000228.1:n.1427+662G>T
NM_000237.3:c.1427+662G>T MANE Select	NP_000228.1:n.1427+662G>T