Canonical Allele Identifier: CA370468399
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954191T>G , CM000670.2:g.19954191T>G GRCh38
NC_000008.10:g.19811702T>G , CM000670.1:g.19811702T>G GRCh37
NC_000008.9:g.19855982T>G NCBI36
NG_008855.1:g.20121T>G
NG_008855.2:g.57475T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.613T>G MANE Select ENSP00000497642.1:p.Phe205Val
ENST00000311322.8:c.613T>G ENSP00000309757.6:p.Phe205Val
NM_000237.2:c.613T>G NP_000228.1:p.Phe205Val
NM_000237.3:c.613T>G MANE Select NP_000228.1:p.Phe205Val