Canonical Allele Identifier: CA1769102042
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954184T= , CM000670.2:g.19954184T= GRCh38
NC_000008.10:g.19811695T= , CM000670.1:g.19811695T= GRCh37
NC_000008.9:g.19855975T= NCBI36
NG_008855.1:g.20114T=
NG_008855.2:g.57468T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.606T= MANE Select ENSP00000497642.1:p.Asp202=
ENST00000311322.8:c.606T= ENSP00000309757.6:p.Asp202=
NM_000237.2:c.606T= NP_000228.1:p.Asp202=
NM_000237.3:c.606T= MANE Select NP_000228.1:p.Asp202=