Canonical Allele Identifier: CA2695208910
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939450_19939451insTTCG , CM000670.2:g.19939450_19939451insTTCG GRCh38
NC_000008.10:g.19796961_19796962insTTCG , CM000670.1:g.19796961_19796962insTTCG GRCh37
NC_000008.9:g.19841241_19841242insTTCG NCBI36
NG_008855.1:g.5380_5381insTTCG
NG_008855.2:g.42734_42735insTTCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.10_11insTTCG MANE Select ENSP00000497642.1:p.Lys4IlefsTer?
ENST00000311322.8:c.10_11insTTCG ENSP00000309757.6:p.Lys4IlefsTer?
ENST00000519773.1:c.10_11insTTCG ENSP00000431028.1:p.Lys4IlefsTer?
ENST00000520959.5:c.-140-8730_-140-8729insTTCG ENSP00000428496.1:n.-140-8730_-140-8729insTTCG
ENST00000521994.1:n.195_196insTTCG
ENST00000522701.5:c.10_11insTTCG ENSP00000428557.1:p.Lys4IlefsTer?
ENST00000523696.1:n.79_80insTTCG
ENST00000524029.5:c.10_11insTTCG ENSP00000428237.1:p.Lys4IlefsTer?
NM_000237.2:c.10_11insTTCG NP_000228.1:p.Lys4IlefsTer?
NM_000237.3:c.10_11insTTCG MANE Select NP_000228.1:p.Lys4IlefsTer?