Canonical Allele Identifier: CA1769083237
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939305T= , CM000670.2:g.19939305T= GRCh38
NC_000008.10:g.19796816T= , CM000670.1:g.19796816T= GRCh37
NC_000008.9:g.19841096T= NCBI36
NG_008855.1:g.5235T=
NG_008855.2:g.42589T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-136T= MANE Select ENSP00000497642.1:n.-136T=
ENST00000311322.8:c.-136T= ENSP00000309757.6:n.-136T=
ENST00000519773.1:c.-136T= ENSP00000431028.1:n.-136T=
ENST00000520959.5:c.-140-8875T= ENSP00000428496.1:n.-140-8875T=
ENST00000521994.1:n.50T=
ENST00000522701.5:c.-136T= ENSP00000428557.1:n.-136T=
ENST00000524029.5:c.-136T= ENSP00000428237.1:n.-136T=
NM_000237.2:c.-136T= NP_000228.1:n.-136T=
NM_000237.3:c.-136T= MANE Select NP_000228.1:n.-136T=