Canonical Allele Identifier: CA1769096909
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951485_19951486delinsCA , CM000670.2:g.19951485_19951486delinsCA GRCh38
NC_000008.10:g.19808996_19808997delinsCA , CM000670.1:g.19808996_19808997delinsCA GRCh37
NC_000008.9:g.19853276_19853277delinsCA NCBI36
NG_008855.1:g.17415_17416delinsCA
NG_008855.2:g.54769_54770delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-284_250-283delinsCA MANE Select ENSP00000497642.1:n.250-284_250-283delinsCA
ENST00000311322.8:c.250-284_250-283delinsCA ENSP00000309757.6:n.250-284_250-283delinsCA
ENST00000520959.5:c.22-284_22-283delinsCA ENSP00000428496.1:n.22-284_22-283delinsCA
ENST00000521994.1:n.435-212_435-211delinsCA
ENST00000522701.5:c.250-284_250-283delinsCA ENSP00000428557.1:n.250-284_250-283delinsCA
ENST00000524029.5:c.250-284_250-283delinsCA ENSP00000428237.1:n.250-284_250-283delinsCA
NM_000237.2:c.250-284_250-283delinsCA NP_000228.1:n.250-284_250-283delinsCA
NM_000237.3:c.250-284_250-283delinsCA MANE Select NP_000228.1:n.250-284_250-283delinsCA