Canonical Allele Identifier: CA1111555607
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2070029601
gnomAD v3: 8-19960600-CA-C
gnomAD v4: 8-19960600-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960603del , CM000670.2:g.19960603del GRCh38
NC_000008.10:g.19818114del , CM000670.1:g.19818114del GRCh37
NC_000008.9:g.19862394del NCBI36
NG_008855.1:g.26533del
NG_008855.2:g.63887del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1140-298del MANE Select ENSP00000497642.1:n.1140-298del
ENST00000650478.1:c.80-298del ENSP00000497560.1:n.80-298del
ENST00000311322.8:c.1140-298del ENSP00000309757.6:n.1140-298del
NM_000237.2:c.1140-298del NP_000228.1:n.1140-298del
NM_000237.3:c.1140-298del MANE Select NP_000228.1:n.1140-298del
Search 100 bp 5'
Search 100 bp 3'