Canonical Allele Identifier: CA1769106886
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957794_19957796delinsTTA , CM000670.2:g.19957794_19957796delinsTTA GRCh38
NC_000008.10:g.19815305_19815307delinsTTA , CM000670.1:g.19815305_19815307delinsTTA GRCh37
NC_000008.9:g.19859585_19859587delinsTTA NCBI36
NG_008855.1:g.23724_23726delinsTTA
NG_008855.2:g.61078_61080delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1466_1019-1464delinsTTA MANE Select ENSP00000497642.1:n.1019-1466_1019-1464delinsTTA
ENST00000650478.1:c.79+1711_79+1713delinsTTA ENSP00000497560.1:n.79+1711_79+1713delinsTTA
ENST00000311322.8:c.1019-1466_1019-1464delinsTTA ENSP00000309757.6:n.1019-1466_1019-1464delinsTTA
NM_000237.2:c.1019-1466_1019-1464delinsTTA NP_000228.1:n.1019-1466_1019-1464delinsTTA
NM_000237.3:c.1019-1466_1019-1464delinsTTA MANE Select NP_000228.1:n.1019-1466_1019-1464delinsTTA