Canonical Allele Identifier: CA370468381
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954183A>C , CM000670.2:g.19954183A>C GRCh38
NC_000008.10:g.19811694A>C , CM000670.1:g.19811694A>C GRCh37
NC_000008.9:g.19855974A>C NCBI36
NG_008855.1:g.20113A>C
NG_008855.2:g.57467A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.605A>C MANE Select ENSP00000497642.1:p.Asp202Ala
ENST00000311322.8:c.605A>C ENSP00000309757.6:p.Asp202Ala
NM_000237.2:c.605A>C NP_000228.1:p.Asp202Ala
NM_000237.3:c.605A>C MANE Select NP_000228.1:p.Asp202Ala