Canonical Allele Identifier: CA1769097195
Gene: LPL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951639A= , CM000670.2:g.19951639A= GRCh38
NC_000008.10:g.19809150A= , CM000670.1:g.19809150A= GRCh37
NC_000008.9:g.19853430A= NCBI36
NG_008855.1:g.17569A=
NG_008855.2:g.54923A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-130A= MANE Select ENSP00000497642.1:n.250-130A=
ENST00000311322.8:c.250-130A= ENSP00000309757.6:n.250-130A=
ENST00000520959.5:c.22-130A= ENSP00000428496.1:n.22-130A=
ENST00000521994.1:n.435-58A=
ENST00000522701.5:c.250-130A= ENSP00000428557.1:n.250-130A=
ENST00000524029.5:c.250-130A= ENSP00000428237.1:n.250-130A=
NM_000237.2:c.250-130A= NP_000228.1:n.250-130A=
NM_000237.3:c.250-130A= MANE Select NP_000228.1:n.250-130A=
Search 100 bp 5'
Search 100 bp 3'