Canonical Allele Identifier: CA1769108016
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958775A= , CM000670.2:g.19958775A= GRCh38
NC_000008.10:g.19816286A= , CM000670.1:g.19816286A= GRCh37
NC_000008.9:g.19860566A= NCBI36
NG_008855.1:g.24705A=
NG_008855.2:g.62059A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-485A= MANE Select ENSP00000497642.1:n.1019-485A=
ENST00000650478.1:c.80-2126A= ENSP00000497560.1:n.80-2126A=
ENST00000311322.8:c.1019-485A= ENSP00000309757.6:n.1019-485A=
NM_000237.2:c.1019-485A= NP_000228.1:n.1019-485A=
NM_000237.3:c.1019-485A= MANE Select NP_000228.1:n.1019-485A=