Canonical Allele Identifier: CA1769101708
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954062C= , CM000670.2:g.19954062C= GRCh38
NC_000008.10:g.19811573C= , CM000670.1:g.19811573C= GRCh37
NC_000008.9:g.19855853C= NCBI36
NG_008855.1:g.19992C=
NG_008855.2:g.57346C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-58C= MANE Select ENSP00000497642.1:n.542-58C=
ENST00000311322.8:c.542-58C= ENSP00000309757.6:n.542-58C=
ENST00000520959.5:c.314-58C= ENSP00000428496.1:n.314-58C=
NM_000237.2:c.542-58C= NP_000228.1:n.542-58C=
NM_000237.3:c.542-58C= MANE Select NP_000228.1:n.542-58C=