Canonical Allele Identifier: CA1769098469
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952186G= , CM000670.2:g.19952186G= GRCh38
NC_000008.10:g.19809697G= , CM000670.1:g.19809697G= GRCh37
NC_000008.9:g.19853977G= NCBI36
NG_008855.1:g.18116G=
NG_008855.2:g.55470G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+238G= MANE Select ENSP00000497642.1:n.429+238G=
ENST00000311322.8:c.429+238G= ENSP00000309757.6:n.429+238G=
ENST00000520959.5:c.201+238G= ENSP00000428496.1:n.201+238G=
NM_000237.2:c.429+238G= NP_000228.1:n.429+238G=
NM_000237.3:c.429+238G= MANE Select NP_000228.1:n.429+238G=
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