Canonical Allele Identifier: CA1769116737
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967027G= , CM000670.2:g.19967027G= GRCh38
NC_000008.10:g.19824538G= , CM000670.1:g.19824538G= GRCh37
NC_000008.9:g.19868818G= NCBI36
NG_008855.1:g.32957G=
NG_008855.2:g.70311G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1717G= MANE Select ENSP00000497642.1:n.*1717G=
ENST00000650478.1:c.2085G= ENSP00000497560.1:n.2085G=
ENST00000311322.8:c.*1717G= ENSP00000309757.6:n.*1717G=
NM_000237.2:c.*1717G= NP_000228.1:n.*1717G=
NM_000237.3:c.*1717G= MANE Select NP_000228.1:n.*1717G=