Canonical Allele Identifier: CA173378100
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs574025999
gnomAD v2: 8-19813097-ACATACT-A
gnomAD v3: 8-19955586-ACATACT-A
gnomAD v4: 8-19955586-ACATACT-A
MyVariant Identifiers: chr8:g.19813098_19813103del (hg19) chr8:g.19955587_19955592del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955591_19955596del , CM000670.2:g.19955591_19955596del GRCh38
NC_000008.10:g.19813102_19813107del , CM000670.1:g.19813102_19813107del GRCh37
NC_000008.9:g.19857382_19857387del NCBI36
NG_008855.1:g.21521_21526del
NG_008855.2:g.58875_58880del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-250_776-245del MANE Select ENSP00000497642.1:n.776-250_776-245del
ENST00000311322.8:c.776-250_776-245del ENSP00000309757.6:n.776-250_776-245del
NM_000237.2:c.776-250_776-245del NP_000228.1:n.776-250_776-245del
NM_000237.3:c.776-250_776-245del MANE Select NP_000228.1:n.776-250_776-245del
Search 100 bp 5'
Search 100 bp 3'