Canonical Allele Identifier: CA1769104327
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955706A= , CM000670.2:g.19955706A= GRCh38
NC_000008.10:g.19813217A= , CM000670.1:g.19813217A= GRCh37
NC_000008.9:g.19857497A= NCBI36
NG_008855.1:g.21636A=
NG_008855.2:g.58990A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-135A= MANE Select ENSP00000497642.1:n.776-135A=
ENST00000311322.8:c.776-135A= ENSP00000309757.6:n.776-135A=
NM_000237.2:c.776-135A= NP_000228.1:n.776-135A=
NM_000237.3:c.776-135A= MANE Select NP_000228.1:n.776-135A=