Canonical Allele Identifier: CA1769097934
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951916C= , CM000670.2:g.19951916C= GRCh38
NC_000008.10:g.19809427C= , CM000670.1:g.19809427C= GRCh37
NC_000008.9:g.19853707C= NCBI36
NG_008855.1:g.17846C=
NG_008855.2:g.55200C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.397C= MANE Select ENSP00000497642.1:p.Gln133=
ENST00000311322.8:c.397C= ENSP00000309757.6:p.Gln133=
ENST00000520959.5:c.169C= ENSP00000428496.1:p.Gln57=
NM_000237.2:c.397C= NP_000228.1:p.Gln133=
NM_000237.3:c.397C= MANE Select NP_000228.1:p.Gln133=