Canonical Allele Identifier: CA1769112362
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962770A= , CM000670.2:g.19962770A= GRCh38
NC_000008.10:g.19820281A= , CM000670.1:g.19820281A= GRCh37
NC_000008.9:g.19864561A= NCBI36
NG_008855.1:g.28700A=
NG_008855.2:g.66054A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1427+551A= MANE Select ENSP00000497642.1:n.1427+551A=
ENST00000650478.1:c.367+551A= ENSP00000497560.1:n.367+551A=
ENST00000311322.8:c.1427+551A= ENSP00000309757.6:n.1427+551A=
NM_000237.2:c.1427+551A= NP_000228.1:n.1427+551A=
NM_000237.3:c.1427+551A= MANE Select NP_000228.1:n.1427+551A=