Canonical Allele Identifier: CA1769106542
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069996362

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957511G>T , CM000670.2:g.19957511G>T GRCh38
NC_000008.10:g.19815022G>T , CM000670.1:g.19815022G>T GRCh37
NC_000008.9:g.19859302G>T NCBI36
NG_008855.1:g.23441G>T
NG_008855.2:g.60795G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1428G>T MANE Select ENSP00000497642.1:n.1018+1428G>T
ENST00000650478.1:c.79+1428G>T ENSP00000497560.1:n.79+1428G>T
ENST00000311322.8:c.1018+1428G>T ENSP00000309757.6:n.1018+1428G>T
NM_000237.2:c.1018+1428G>T NP_000228.1:n.1018+1428G>T
NM_000237.3:c.1018+1428G>T MANE Select NP_000228.1:n.1018+1428G>T