Canonical Allele Identifier: CA1769104773
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956039G= , CM000670.2:g.19956039G= GRCh38
NC_000008.10:g.19813550G= , CM000670.1:g.19813550G= GRCh37
NC_000008.9:g.19857830G= NCBI36
NG_008855.1:g.21969G=
NG_008855.2:g.59323G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.974G= MANE Select ENSP00000497642.1:p.Ser325=
ENST00000650478.1:c.35G= ENSP00000497560.1:p.Ser12=
ENST00000311322.8:c.974G= ENSP00000309757.6:p.Ser325=
NM_000237.2:c.974G= NP_000228.1:p.Ser325=
NM_000237.3:c.974G= MANE Select NP_000228.1:p.Ser325=