Canonical Allele Identifier: CA1769107180
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070002688
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958033_19958034insCTATTTATTTAT , CM000670.2:g.19958033_19958034insCTATTTATTTAT GRCh38
NC_000008.10:g.19815544_19815545insCTATTTATTTAT , CM000670.1:g.19815544_19815545insCTATTTATTTAT GRCh37
NC_000008.9:g.19859824_19859825insCTATTTATTTAT NCBI36
NG_008855.1:g.23963_23964insCTATTTATTTAT
NG_008855.2:g.61317_61318insCTATTTATTTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1227_1019-1226insCTATTTATTTAT MANE Select ENSP00000497642.1:n.1019-1227_1019-1226insCTATTTATTTAT
ENST00000650478.1:c.79+1950_79+1951insCTATTTATTTAT ENSP00000497560.1:n.79+1950_79+1951insCTATTTATTTAT
ENST00000311322.8:c.1019-1227_1019-1226insCTATTTATTTAT ENSP00000309757.6:n.1019-1227_1019-1226insCTATTTATTTAT
NM_000237.2:c.1019-1227_1019-1226insCTATTTATTTAT NP_000228.1:n.1019-1227_1019-1226insCTATTTATTTAT
NM_000237.3:c.1019-1227_1019-1226insCTATTTATTTAT MANE Select NP_000228.1:n.1019-1227_1019-1226insCTATTTATTTAT
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