Canonical Allele Identifier: CA1111553725
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070010734
gnomAD v3: 8-19958805-G-T
gnomAD v4: 8-19958805-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958805G>T , CM000670.2:g.19958805G>T GRCh38
NC_000008.10:g.19816316G>T , CM000670.1:g.19816316G>T GRCh37
NC_000008.9:g.19860596G>T NCBI36
NG_008855.1:g.24735G>T
NG_008855.2:g.62089G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-455G>T MANE Select ENSP00000497642.1:n.1019-455G>T
ENST00000650478.1:c.80-2096G>T ENSP00000497560.1:n.80-2096G>T
ENST00000311322.8:c.1019-455G>T ENSP00000309757.6:n.1019-455G>T
NM_000237.2:c.1019-455G>T NP_000228.1:n.1019-455G>T
NM_000237.3:c.1019-455G>T MANE Select NP_000228.1:n.1019-455G>T