Canonical Allele Identifier: CA370468316
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954149T>A , CM000670.2:g.19954149T>A GRCh38
NC_000008.10:g.19811660T>A , CM000670.1:g.19811660T>A GRCh37
NC_000008.9:g.19855940T>A NCBI36
NG_008855.1:g.20079T>A
NG_008855.2:g.57433T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.571T>A MANE Select ENSP00000497642.1:p.Tyr191Asn
ENST00000311322.8:c.571T>A ENSP00000309757.6:p.Tyr191Asn
ENST00000520959.5:c.343T>A ENSP00000428496.1:p.Tyr115Asn
NM_000237.2:c.571T>A NP_000228.1:p.Tyr191Asn
NM_000237.3:c.571T>A MANE Select NP_000228.1:p.Tyr191Asn