Canonical Allele Identifier: CA4655648

Gene: LPL

Linked Data

• dbSNP Id: rs541807762
• ExAC: 8:19818376 T / G
• gnomAD v2: 8-19818376-T-G
• gnomAD v3: 8-19960865-T-G
• gnomAD v4: 8-19960865-T-G
• MyVariant Identifiers: chr8:g.19818376T>G (hg19) ; chr8:g.19960865T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960865T>G , CM000670.2:g.19960865T>G	GRCh38
NC_000008.10:g.19818376T>G , CM000670.1:g.19818376T>G	GRCh37
NC_000008.9:g.19862656T>G	NCBI36
NG_008855.1:g.26795T>G
NG_008855.2:g.64149T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1140-36T>G MANE Select	ENSP00000497642.1:n.1140-36T>G
ENST00000650478.1:c.80-36T>G	ENSP00000497560.1:n.80-36T>G
ENST00000311322.8:c.1140-36T>G	ENSP00000309757.6:n.1140-36T>G
NM_000237.2:c.1140-36T>G	NP_000228.1:n.1140-36T>G
NM_000237.3:c.1140-36T>G MANE Select	NP_000228.1:n.1140-36T>G