Canonical Allele Identifier: CA1769097632
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951825A= , CM000670.2:g.19951825A= GRCh38
NC_000008.10:g.19809336A= , CM000670.1:g.19809336A= GRCh37
NC_000008.9:g.19853616A= NCBI36
NG_008855.1:g.17755A=
NG_008855.2:g.55109A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.306A= MANE Select ENSP00000497642.1:p.Arg102=
ENST00000311322.8:c.306A= ENSP00000309757.6:p.Arg102=
ENST00000520959.5:c.78A= ENSP00000428496.1:p.Arg26=
ENST00000521994.1:n.563A=
ENST00000522701.5:c.306A= ENSP00000428557.1:p.Arg102=
ENST00000524029.5:c.306A= ENSP00000428237.1:p.Arg102=
NM_000237.2:c.306A= NP_000228.1:p.Arg102=
NM_000237.3:c.306A= MANE Select NP_000228.1:p.Arg102=