Canonical Allele Identifier: CA1769083204
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939273_19939276delinsTTCC , CM000670.2:g.19939273_19939276delinsTTCC GRCh38
NC_000008.10:g.19796784_19796787delinsTTCC , CM000670.1:g.19796784_19796787delinsTTCC GRCh37
NC_000008.9:g.19841064_19841067delinsTTCC NCBI36
NG_008855.1:g.5203_5206delinsTTCC
NG_008855.2:g.42557_42560delinsTTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-168_-165delinsTTCC MANE Select ENSP00000497642.1:n.-168_-165delinsTTCC
ENST00000311322.8:c.-168_-165delinsTTCC ENSP00000309757.6:n.-168_-165delinsTTCC
ENST00000519773.1:c.-168_-165delinsTTCC ENSP00000431028.1:n.-168_-165delinsTTCC
ENST00000520959.5:c.-140-8907_-140-8904delinsTTCC ENSP00000428496.1:n.-140-8907_-140-8904delinsTTCC
ENST00000521994.1:n.18_21delinsTTCC
ENST00000522701.5:c.-168_-165delinsTTCC ENSP00000428557.1:n.-168_-165delinsTTCC
ENST00000524029.5:c.-153-15_-153-12delinsTTCC ENSP00000428237.1:n.-153-15_-153-12delinsTTCC
NM_000237.2:c.-168_-165delinsTTCC NP_000228.1:n.-168_-165delinsTTCC
NM_000237.3:c.-168_-165delinsTTCC MANE Select NP_000228.1:n.-168_-165delinsTTCC