Canonical Allele Identifier: CA1769096969
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951506A= , CM000670.2:g.19951506A= GRCh38
NC_000008.10:g.19809017A= , CM000670.1:g.19809017A= GRCh37
NC_000008.9:g.19853297A= NCBI36
NG_008855.1:g.17436A=
NG_008855.2:g.54790A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-263A= MANE Select ENSP00000497642.1:n.250-263A=
ENST00000311322.8:c.250-263A= ENSP00000309757.6:n.250-263A=
ENST00000520959.5:c.22-263A= ENSP00000428496.1:n.22-263A=
ENST00000521994.1:n.435-191A=
ENST00000522701.5:c.250-263A= ENSP00000428557.1:n.250-263A=
ENST00000524029.5:c.250-263A= ENSP00000428237.1:n.250-263A=
NM_000237.2:c.250-263A= NP_000228.1:n.250-263A=
NM_000237.3:c.250-263A= MANE Select NP_000228.1:n.250-263A=
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