Canonical Allele Identifier: CA918215068

Gene: LPL

Linked Data

• dbSNP Id: rs1554516247

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939272_19939273insCC , CM000670.2:g.19939272_19939273insCC	GRCh38
NC_000008.10:g.19796783_19796784insCC , CM000670.1:g.19796783_19796784insCC	GRCh37
NC_000008.9:g.19841063_19841064insCC	NCBI36
NG_008855.1:g.5202_5203insCC
NG_008855.2:g.42556_42557insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-169_-168insCC MANE Select	ENSP00000497642.1:n.-169_-168insCC
ENST00000311322.8:c.-169_-168insCC	ENSP00000309757.6:n.-169_-168insCC
ENST00000519773.1:c.-169_-168insCC	ENSP00000431028.1:n.-169_-168insCC
ENST00000520959.5:c.-140-8908_-140-8907insCC	ENSP00000428496.1:n.-140-8908_-140-8907insCC
ENST00000521994.1:n.17_18insCC
ENST00000522701.5:c.-169_-168insCC	ENSP00000428557.1:n.-169_-168insCC
ENST00000524029.5:c.-153-16_-153-15insCC	ENSP00000428237.1:n.-153-16_-153-15insCC
NM_000237.2:c.-169_-168insCC	NP_000228.1:n.-169_-168insCC
NM_000237.3:c.-169_-168insCC MANE Select	NP_000228.1:n.-169_-168insCC