Canonical Allele Identifier: CA370468393
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954188G>T , CM000670.2:g.19954188G>T GRCh38
NC_000008.10:g.19811699G>T , CM000670.1:g.19811699G>T GRCh37
NC_000008.9:g.19855979G>T NCBI36
NG_008855.1:g.20118G>T
NG_008855.2:g.57472G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.610G>T MANE Select ENSP00000497642.1:p.Asp204Tyr
ENST00000311322.8:c.610G>T ENSP00000309757.6:p.Asp204Tyr
NM_000237.2:c.610G>T NP_000228.1:p.Asp204Tyr
NM_000237.3:c.610G>T MANE Select NP_000228.1:p.Asp204Tyr