Canonical Allele Identifier: CA1769110700
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960951T= , CM000670.2:g.19960951T= GRCh38
NC_000008.10:g.19818462T= , CM000670.1:g.19818462T= GRCh37
NC_000008.9:g.19862742T= NCBI36
NG_008855.1:g.26881T=
NG_008855.2:g.64235T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1190T= MANE Select ENSP00000497642.1:p.Val397=
ENST00000650478.1:c.130T= ENSP00000497560.1:n.130T=
ENST00000311322.8:c.1190T= ENSP00000309757.6:p.Val397=
NM_000237.2:c.1190T= NP_000228.1:p.Val397=
NM_000237.3:c.1190T= MANE Select NP_000228.1:p.Val397=