Canonical Allele Identifier: CA1769101713
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069960617

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954064A>T , CM000670.2:g.19954064A>T GRCh38
NC_000008.10:g.19811575A>T , CM000670.1:g.19811575A>T GRCh37
NC_000008.9:g.19855855A>T NCBI36
NG_008855.1:g.19994A>T
NG_008855.2:g.57348A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-56A>T MANE Select ENSP00000497642.1:n.542-56A>T
ENST00000311322.8:c.542-56A>T ENSP00000309757.6:n.542-56A>T
ENST00000520959.5:c.314-56A>T ENSP00000428496.1:n.314-56A>T
NM_000237.2:c.542-56A>T NP_000228.1:n.542-56A>T
NM_000237.3:c.542-56A>T MANE Select NP_000228.1:n.542-56A>T