Canonical Allele Identifier: CA1769108020
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958776C= , CM000670.2:g.19958776C= GRCh38
NC_000008.10:g.19816287C= , CM000670.1:g.19816287C= GRCh37
NC_000008.9:g.19860567C= NCBI36
NG_008855.1:g.24706C=
NG_008855.2:g.62060C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-484C= MANE Select ENSP00000497642.1:n.1019-484C=
ENST00000650478.1:c.80-2125C= ENSP00000497560.1:n.80-2125C=
ENST00000311322.8:c.1019-484C= ENSP00000309757.6:n.1019-484C=
NM_000237.2:c.1019-484C= NP_000228.1:n.1019-484C=
NM_000237.3:c.1019-484C= MANE Select NP_000228.1:n.1019-484C=