Canonical Allele Identifier: CA370468512
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954246T>C , CM000670.2:g.19954246T>C GRCh38
NC_000008.10:g.19811757T>C , CM000670.1:g.19811757T>C GRCh37
NC_000008.9:g.19856037T>C NCBI36
NG_008855.1:g.20176T>C
NG_008855.2:g.57530T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.668T>C MANE Select ENSP00000497642.1:p.Ile223Thr
ENST00000311322.8:c.668T>C ENSP00000309757.6:p.Ile223Thr
NM_000237.2:c.668T>C NP_000228.1:p.Ile223Thr
NM_000237.3:c.668T>C MANE Select NP_000228.1:p.Ile223Thr