Canonical Allele Identifier: CA370468408
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954194G>C , CM000670.2:g.19954194G>C GRCh38
NC_000008.10:g.19811705G>C , CM000670.1:g.19811705G>C GRCh37
NC_000008.9:g.19855985G>C NCBI36
NG_008855.1:g.20124G>C
NG_008855.2:g.57478G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.616G>C MANE Select ENSP00000497642.1:p.Val206Leu
ENST00000311322.8:c.616G>C ENSP00000309757.6:p.Val206Leu
NM_000237.2:c.616G>C NP_000228.1:p.Val206Leu
NM_000237.3:c.616G>C MANE Select NP_000228.1:p.Val206Leu