Canonical Allele Identifier: CA370468576
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954276A>G , CM000670.2:g.19954276A>G GRCh38
NC_000008.10:g.19811787A>G , CM000670.1:g.19811787A>G GRCh37
NC_000008.9:g.19856067A>G NCBI36
NG_008855.1:g.20206A>G
NG_008855.2:g.57560A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.698A>G MANE Select ENSP00000497642.1:p.Tyr233Cys
ENST00000311322.8:c.698A>G ENSP00000309757.6:p.Tyr233Cys
NM_000237.2:c.698A>G NP_000228.1:p.Tyr233Cys
NM_000237.3:c.698A>G MANE Select NP_000228.1:p.Tyr233Cys