Canonical Allele Identifier: CA4655470
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs778308749
gnomAD v2: 8-19811660-T-G
gnomAD v4: 8-19954149-T-G

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.571T>G MANE Select ENSP00000497642.1:p.Tyr191Asp
ENST00000311322.8:c.571T>G ENSP00000309757.6:p.Tyr191Asp
ENST00000520959.5:c.343T>G ENSP00000428496.1:p.Tyr115Asp
NM_000237.2:c.571T>G NP_000228.1:p.Tyr191Asp
NM_000237.3:c.571T>G MANE Select NP_000228.1:p.Tyr191Asp