Canonical Allele Identifier: CA370467779
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19809457G>C (hg19) chr8:g.19951946G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951946G>C , CM000670.2:g.19951946G>C GRCh38
NC_000008.10:g.19809457G>C , CM000670.1:g.19809457G>C GRCh37
NC_000008.9:g.19853737G>C NCBI36
NG_008855.1:g.17876G>C
NG_008855.2:g.55230G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.427G>C MANE Select ENSP00000497642.1:p.Glu143Gln
ENST00000311322.8:c.427G>C ENSP00000309757.6:p.Glu143Gln
ENST00000520959.5:c.199G>C ENSP00000428496.1:p.Glu67Gln
NM_000237.2:c.427G>C NP_000228.1:p.Glu143Gln
NM_000237.3:c.427G>C MANE Select NP_000228.1:p.Glu143Gln
Search 100 bp 5'
Search 100 bp 3'