Canonical Allele Identifier: CA2779304305
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962026T>C , CM000670.2:g.19962026T>C GRCh38
NC_000008.10:g.19819537T>C , CM000670.1:g.19819537T>C GRCh37
NC_000008.9:g.19863817T>C NCBI36
NG_008855.1:g.27956T>C
NG_008855.2:g.65310T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1323-89T>C MANE Select ENSP00000497642.1:n.1323-89T>C
ENST00000650478.1:c.263-89T>C ENSP00000497560.1:n.263-89T>C
ENST00000311322.8:c.1323-89T>C ENSP00000309757.6:n.1323-89T>C
NM_000237.2:c.1323-89T>C NP_000228.1:n.1323-89T>C
NM_000237.3:c.1323-89T>C MANE Select NP_000228.1:n.1323-89T>C