Canonical Allele Identifier: CA2779304344
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962843G>T , CM000670.2:g.19962843G>T GRCh38
NC_000008.10:g.19820354G>T , CM000670.1:g.19820354G>T GRCh37
NC_000008.9:g.19864634G>T NCBI36
NG_008855.1:g.28773G>T
NG_008855.2:g.66127G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1427+624G>T MANE Select ENSP00000497642.1:n.1427+624G>T
ENST00000650478.1:c.367+624G>T ENSP00000497560.1:n.367+624G>T
ENST00000311322.8:c.1427+624G>T ENSP00000309757.6:n.1427+624G>T
NM_000237.2:c.1427+624G>T NP_000228.1:n.1427+624G>T
NM_000237.3:c.1427+624G>T MANE Select NP_000228.1:n.1427+624G>T