Canonical Allele Identifier: CA1769116695
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966981T= , CM000670.2:g.19966981T= GRCh38
NC_000008.10:g.19824492T= , CM000670.1:g.19824492T= GRCh37
NC_000008.9:g.19868772T= NCBI36
NG_008855.1:g.32911T=
NG_008855.2:g.70265T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1671T= MANE Select ENSP00000497642.1:n.*1671T=
ENST00000650478.1:c.2039T= ENSP00000497560.1:n.2039T=
ENST00000311322.8:c.*1671T= ENSP00000309757.6:n.*1671T=
NM_000237.2:c.*1671T= NP_000228.1:n.*1671T=
NM_000237.3:c.*1671T= MANE Select NP_000228.1:n.*1671T=