Canonical Allele Identifier: CA580154197

Gene: LPL

Linked Data

• dbSNP Id: rs1028935900
• gnomAD v2: 8-19796784-T-TTCC
• gnomAD v3: 8-19939273-T-TTCC
• gnomAD v4: 8-19939273-T-TTCC
• MyVariant Identifiers: chr8:g.19796784_19796785insTCC (hg19) ; chr8:g.19939273_19939274insTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939282_19939284dup , CM000670.2:g.19939282_19939284dup	GRCh38
NC_000008.10:g.19796793_19796795dup , CM000670.1:g.19796793_19796795dup	GRCh37
NC_000008.9:g.19841073_19841075dup	NCBI36
NG_008855.1:g.5212_5214dup
NG_008855.2:g.42566_42568dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-159_-157dup MANE Select	ENSP00000497642.1:n.-159_-157dup
ENST00000311322.8:c.-159_-157dup	ENSP00000309757.6:n.-159_-157dup
ENST00000519773.1:c.-159_-157dup	ENSP00000431028.1:n.-159_-157dup
ENST00000520959.5:c.-140-8898_-140-8896dup	ENSP00000428496.1:n.-140-8898_-140-8896dup
ENST00000521994.1:n.27_29dup
ENST00000522701.5:c.-159_-157dup	ENSP00000428557.1:n.-159_-157dup
ENST00000524029.5:c.-153-6_-153-4dup	ENSP00000428237.1:n.-153-6_-153-4dup
NM_000237.2:c.-159_-157dup	NP_000228.1:n.-159_-157dup
NM_000237.3:c.-159_-157dup MANE Select	NP_000228.1:n.-159_-157dup