Canonical Allele Identifier: CA1769106659
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957590A= , CM000670.2:g.19957590A= GRCh38
NC_000008.10:g.19815101A= , CM000670.1:g.19815101A= GRCh37
NC_000008.9:g.19859381A= NCBI36
NG_008855.1:g.23520A=
NG_008855.2:g.60874A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1507A= MANE Select ENSP00000497642.1:p.=
ENST00000650478.1:n.79+1507A= ENSP00000497560.1:p.=
ENST00000311322.8:c.1018+1507A= ENSP00000309757.6:p.=
NM_000237.2:c.1018+1507A= NP_000228.1:p.=
NM_000237.3:c.1018+1507A= MANE Select NP_000228.1:p.=