Canonical Allele Identifier: CA1769116773
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967057C= , CM000670.2:g.19967057C= GRCh38
NC_000008.10:g.19824568C= , CM000670.1:g.19824568C= GRCh37
NC_000008.9:g.19868848C= NCBI36
NG_008855.1:g.32987C=
NG_008855.2:g.70341C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1747C= MANE Select ENSP00000497642.1:n.*1747C=
ENST00000650478.1:c.2115C= ENSP00000497560.1:n.2115C=
ENST00000311322.8:c.*1747C= ENSP00000309757.6:n.*1747C=
NM_000237.2:c.*1747C= NP_000228.1:n.*1747C=
NM_000237.3:c.*1747C= MANE Select NP_000228.1:n.*1747C=