Canonical Allele Identifier: CA1769104782
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956041A= , CM000670.2:g.19956041A= GRCh38
NC_000008.10:g.19813552A= , CM000670.1:g.19813552A= GRCh37
NC_000008.9:g.19857832A= NCBI36
NG_008855.1:g.21971A=
NG_008855.2:g.59325A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.976A= MANE Select ENSP00000497642.1:p.Ser326=
ENST00000650478.1:c.37A= ENSP00000497560.1:p.Ser13=
ENST00000311322.8:c.976A= ENSP00000309757.6:p.Ser326=
NM_000237.2:c.976A= NP_000228.1:p.Ser326=
NM_000237.3:c.976A= MANE Select NP_000228.1:p.Ser326=