Canonical Allele Identifier: CA1769097188
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951627_19951629delinsTTC , CM000670.2:g.19951627_19951629delinsTTC GRCh38
NC_000008.10:g.19809138_19809140delinsTTC , CM000670.1:g.19809138_19809140delinsTTC GRCh37
NC_000008.9:g.19853418_19853420delinsTTC NCBI36
NG_008855.1:g.17557_17559delinsTTC
NG_008855.2:g.54911_54913delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-142_250-140delinsTTC MANE Select ENSP00000497642.1:n.250-142_250-140delinsTTC
ENST00000311322.8:c.250-142_250-140delinsTTC ENSP00000309757.6:n.250-142_250-140delinsTTC
ENST00000520959.5:c.22-142_22-140delinsTTC ENSP00000428496.1:n.22-142_22-140delinsTTC
ENST00000521994.1:n.435-70_435-68delinsTTC
ENST00000522701.5:c.250-142_250-140delinsTTC ENSP00000428557.1:n.250-142_250-140delinsTTC
ENST00000524029.5:c.250-142_250-140delinsTTC ENSP00000428237.1:n.250-142_250-140delinsTTC
NM_000237.2:c.250-142_250-140delinsTTC NP_000228.1:n.250-142_250-140delinsTTC
NM_000237.3:c.250-142_250-140delinsTTC MANE Select NP_000228.1:n.250-142_250-140delinsTTC