Canonical Allele Identifier: CA370468568
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954272A>C , CM000670.2:g.19954272A>C GRCh38
NC_000008.10:g.19811783A>C , CM000670.1:g.19811783A>C GRCh37
NC_000008.9:g.19856063A>C NCBI36
NG_008855.1:g.20202A>C
NG_008855.2:g.57556A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.694A>C MANE Select ENSP00000497642.1:p.Ile232Leu
ENST00000311322.8:c.694A>C ENSP00000309757.6:p.Ile232Leu
NM_000237.2:c.694A>C NP_000228.1:p.Ile232Leu
NM_000237.3:c.694A>C MANE Select NP_000228.1:p.Ile232Leu