Canonical Allele Identifier: CA1769110701
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960952A= , CM000670.2:g.19960952A= GRCh38
NC_000008.10:g.19818463A= , CM000670.1:g.19818463A= GRCh37
NC_000008.9:g.19862743A= NCBI36
NG_008855.1:g.26882A=
NG_008855.2:g.64236A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1191A= MANE Select ENSP00000497642.1:p.Val397=
ENST00000650478.1:c.131A= ENSP00000497560.1:n.131A=
ENST00000311322.8:c.1191A= ENSP00000309757.6:p.Val397=
NM_000237.2:c.1191A= NP_000228.1:p.Val397=
NM_000237.3:c.1191A= MANE Select NP_000228.1:p.Val397=