Canonical Allele Identifier: CA1769102659
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954256A= , CM000670.2:g.19954256A= GRCh38
NC_000008.10:g.19811767A= , CM000670.1:g.19811767A= GRCh37
NC_000008.9:g.19856047A= NCBI36
NG_008855.1:g.20186A=
NG_008855.2:g.57540A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.678A= MANE Select ENSP00000497642.1:p.Pro226=
ENST00000311322.8:c.678A= ENSP00000309757.6:p.Pro226=
NM_000237.2:c.678A= NP_000228.1:p.Pro226=
NM_000237.3:c.678A= MANE Select NP_000228.1:p.Pro226=