Canonical Allele Identifier: CA1769101863
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954126A= , CM000670.2:g.19954126A= GRCh38
NC_000008.10:g.19811637A= , CM000670.1:g.19811637A= GRCh37
NC_000008.9:g.19855917A= NCBI36
NG_008855.1:g.20056A=
NG_008855.2:g.57410A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.548A= MANE Select ENSP00000497642.1:p.Asp183=
ENST00000311322.8:c.548A= ENSP00000309757.6:p.Asp183=
ENST00000520959.5:c.320A= ENSP00000428496.1:p.Asp107=
NM_000237.2:c.548A= NP_000228.1:p.Asp183=
NM_000237.3:c.548A= MANE Select NP_000228.1:p.Asp183=