Canonical Allele Identifier: CA4655675
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs757705770
gnomAD v2: 8-19818502-G-C
gnomAD v4: 8-19960991-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960991G>C , CM000670.2:g.19960991G>C GRCh38
NC_000008.10:g.19818502G>C , CM000670.1:g.19818502G>C GRCh37
NC_000008.9:g.19862782G>C NCBI36
NG_008855.1:g.26921G>C
NG_008855.2:g.64275G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1230G>C MANE Select ENSP00000497642.1:p.Lys410Asn
ENST00000650478.1:c.170G>C ENSP00000497560.1:n.170G>C
ENST00000311322.8:c.1230G>C ENSP00000309757.6:p.Lys410Asn
NM_000237.2:c.1230G>C NP_000228.1:p.Lys410Asn
NM_000237.3:c.1230G>C MANE Select NP_000228.1:p.Lys410Asn