Canonical Allele Identifier: CA918214963
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1554517889

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958037_19958038insATTT , CM000670.2:g.19958037_19958038insATTT GRCh38
NC_000008.10:g.19815548_19815549insATTT , CM000670.1:g.19815548_19815549insATTT GRCh37
NC_000008.9:g.19859828_19859829insATTT NCBI36
NG_008855.1:g.23967_23968insATTT
NG_008855.2:g.61321_61322insATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1223_1019-1222insATTT MANE Select ENSP00000497642.1:n.1019-1223_1019-1222insATTT
ENST00000650478.1:c.79+1954_79+1955insATTT ENSP00000497560.1:n.79+1954_79+1955insATTT
ENST00000311322.8:c.1019-1223_1019-1222insATTT ENSP00000309757.6:n.1019-1223_1019-1222insATTT
NM_000237.2:c.1019-1223_1019-1222insATTT NP_000228.1:n.1019-1223_1019-1222insATTT
NM_000237.3:c.1019-1223_1019-1222insATTT MANE Select NP_000228.1:n.1019-1223_1019-1222insATTT