Canonical Allele Identifier: CA370638519
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960900G>C , CM000670.2:g.19960900G>C GRCh38
NC_000008.10:g.19818411G>C , CM000670.1:g.19818411G>C GRCh37
NC_000008.9:g.19862691G>C NCBI36
NG_008855.1:g.26830G>C
NG_008855.2:g.64184G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1140-1G>C MANE Select ENSP00000497642.1:n.1140-1G>C
ENST00000650478.1:c.80-1G>C ENSP00000497560.1:n.80-1G>C
ENST00000311322.8:c.1140-1G>C ENSP00000309757.6:n.1140-1G>C
NM_000237.2:c.1140-1G>C NP_000228.1:n.1140-1G>C
NM_000237.3:c.1140-1G>C MANE Select NP_000228.1:n.1140-1G>C