Canonical Allele Identifier: CA370468589
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19954282-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954282A>G , CM000670.2:g.19954282A>G GRCh38
NC_000008.10:g.19811793A>G , CM000670.1:g.19811793A>G GRCh37
NC_000008.9:g.19856073A>G NCBI36
NG_008855.1:g.20212A>G
NG_008855.2:g.57566A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.704A>G MANE Select ENSP00000497642.1:p.Asn235Ser
ENST00000311322.8:c.704A>G ENSP00000309757.6:p.Asn235Ser
NM_000237.2:c.704A>G NP_000228.1:p.Asn235Ser
NM_000237.3:c.704A>G MANE Select NP_000228.1:p.Asn235Ser