Canonical Allele Identifier: CA1769101940
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954151T= , CM000670.2:g.19954151T= GRCh38
NC_000008.10:g.19811662T= , CM000670.1:g.19811662T= GRCh37
NC_000008.9:g.19855942T= NCBI36
NG_008855.1:g.20081T=
NG_008855.2:g.57435T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.573T= MANE Select ENSP00000497642.1:p.Tyr191=
ENST00000311322.8:c.573T= ENSP00000309757.6:p.Tyr191=
ENST00000520959.5:c.345T= ENSP00000428496.1:p.Tyr115=
NM_000237.2:c.573T= NP_000228.1:p.Tyr191=
NM_000237.3:c.573T= MANE Select NP_000228.1:p.Tyr191=