Canonical Allele Identifier: CA370468521
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954249A>C , CM000670.2:g.19954249A>C GRCh38
NC_000008.10:g.19811760A>C , CM000670.1:g.19811760A>C GRCh37
NC_000008.9:g.19856040A>C NCBI36
NG_008855.1:g.20179A>C
NG_008855.2:g.57533A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.671A>C MANE Select ENSP00000497642.1:p.Gln224Pro
ENST00000311322.8:c.671A>C ENSP00000309757.6:p.Gln224Pro
NM_000237.2:c.671A>C NP_000228.1:p.Gln224Pro
NM_000237.3:c.671A>C MANE Select NP_000228.1:p.Gln224Pro