Canonical Allele Identifier: CA370468272
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954128C>A , CM000670.2:g.19954128C>A GRCh38
NC_000008.10:g.19811639C>A , CM000670.1:g.19811639C>A GRCh37
NC_000008.9:g.19855919C>A NCBI36
NG_008855.1:g.20058C>A
NG_008855.2:g.57412C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.550C>A MANE Select ENSP00000497642.1:p.Pro184Thr
ENST00000311322.8:c.550C>A ENSP00000309757.6:p.Pro184Thr
ENST00000520959.5:c.322C>A ENSP00000428496.1:p.Pro108Thr
NM_000237.2:c.550C>A NP_000228.1:p.Pro184Thr
NM_000237.3:c.550C>A MANE Select NP_000228.1:p.Pro184Thr