Canonical Allele Identifier: CA1769110358
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960612_19960613delinsGA , CM000670.2:g.19960612_19960613delinsGA GRCh38
NC_000008.10:g.19818123_19818124delinsGA , CM000670.1:g.19818123_19818124delinsGA GRCh37
NC_000008.9:g.19862403_19862404delinsGA NCBI36
NG_008855.1:g.26542_26543delinsGA
NG_008855.2:g.63896_63897delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1140-289_1140-288delinsGA MANE Select ENSP00000497642.1:n.1140-289_1140-288delinsGA
ENST00000650478.1:c.80-289_80-288delinsGA ENSP00000497560.1:n.80-289_80-288delinsGA
ENST00000311322.8:c.1140-289_1140-288delinsGA ENSP00000309757.6:n.1140-289_1140-288delinsGA
NM_000237.2:c.1140-289_1140-288delinsGA NP_000228.1:n.1140-289_1140-288delinsGA
NM_000237.3:c.1140-289_1140-288delinsGA MANE Select NP_000228.1:n.1140-289_1140-288delinsGA