Canonical Allele Identifier: CA1769104195
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955574A= , CM000670.2:g.19955574A= GRCh38
NC_000008.10:g.19813085A= , CM000670.1:g.19813085A= GRCh37
NC_000008.9:g.19857365A= NCBI36
NG_008855.1:g.21504A=
NG_008855.2:g.58858A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-267A= MANE Select ENSP00000497642.1:n.776-267A=
ENST00000311322.8:c.776-267A= ENSP00000309757.6:n.776-267A=
NM_000237.2:c.776-267A= NP_000228.1:n.776-267A=
NM_000237.3:c.776-267A= MANE Select NP_000228.1:n.776-267A=
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