Canonical Allele Identifier: CA370467756
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951938A>G , CM000670.2:g.19951938A>G GRCh38
NC_000008.10:g.19809449A>G , CM000670.1:g.19809449A>G GRCh37
NC_000008.9:g.19853729A>G NCBI36
NG_008855.1:g.17868A>G
NG_008855.2:g.55222A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.419A>G MANE Select ENSP00000497642.1:p.Asn140Ser
ENST00000311322.8:c.419A>G ENSP00000309757.6:p.Asn140Ser
ENST00000520959.5:c.191A>G ENSP00000428496.1:p.Asn64Ser
NM_000237.2:c.419A>G NP_000228.1:p.Asn140Ser
NM_000237.3:c.419A>G MANE Select NP_000228.1:p.Asn140Ser