Canonical Allele Identifier: CA370467516
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951826G>C , CM000670.2:g.19951826G>C GRCh38
NC_000008.10:g.19809337G>C , CM000670.1:g.19809337G>C GRCh37
NC_000008.9:g.19853617G>C NCBI36
NG_008855.1:g.17756G>C
NG_008855.2:g.55110G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.307G>C MANE Select ENSP00000497642.1:p.Glu103Gln
ENST00000311322.8:c.307G>C ENSP00000309757.6:p.Glu103Gln
ENST00000520959.5:c.79G>C ENSP00000428496.1:p.Glu27Gln
ENST00000521994.1:n.564G>C
ENST00000522701.5:c.307G>C ENSP00000428557.1:p.Glu103Gln
ENST00000524029.5:c.307G>C ENSP00000428237.1:p.Glu103Gln
NM_000237.2:c.307G>C NP_000228.1:p.Glu103Gln
NM_000237.3:c.307G>C MANE Select NP_000228.1:p.Glu103Gln