Canonical Allele Identifier: CA370468379
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954182G>C , CM000670.2:g.19954182G>C GRCh38
NC_000008.10:g.19811693G>C , CM000670.1:g.19811693G>C GRCh37
NC_000008.9:g.19855973G>C NCBI36
NG_008855.1:g.20112G>C
NG_008855.2:g.57466G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.604G>C MANE Select ENSP00000497642.1:p.Asp202His
ENST00000311322.8:c.604G>C ENSP00000309757.6:p.Asp202His
NM_000237.2:c.604G>C NP_000228.1:p.Asp202His
NM_000237.3:c.604G>C MANE Select NP_000228.1:p.Asp202His