Canonical Allele Identifier: CA1769101887
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954128C= , CM000670.2:g.19954128C= GRCh38
NC_000008.10:g.19811639C= , CM000670.1:g.19811639C= GRCh37
NC_000008.9:g.19855919C= NCBI36
NG_008855.1:g.20058C=
NG_008855.2:g.57412C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.550C= MANE Select ENSP00000497642.1:p.Pro184=
ENST00000311322.8:c.550C= ENSP00000309757.6:p.Pro184=
ENST00000520959.5:c.322C= ENSP00000428496.1:p.Pro108=
NM_000237.2:c.550C= NP_000228.1:p.Pro184=
NM_000237.3:c.550C= MANE Select NP_000228.1:p.Pro184=