Canonical Allele Identifier: CA370468395
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954189A>G , CM000670.2:g.19954189A>G GRCh38
NC_000008.10:g.19811700A>G , CM000670.1:g.19811700A>G GRCh37
NC_000008.9:g.19855980A>G NCBI36
NG_008855.1:g.20119A>G
NG_008855.2:g.57473A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.611A>G MANE Select ENSP00000497642.1:p.Asp204Gly
ENST00000311322.8:c.611A>G ENSP00000309757.6:p.Asp204Gly
NM_000237.2:c.611A>G NP_000228.1:p.Asp204Gly
NM_000237.3:c.611A>G MANE Select NP_000228.1:p.Asp204Gly