Canonical Allele Identifier: CA1769097663
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951830C= , CM000670.2:g.19951830C= GRCh38
NC_000008.10:g.19809341C= , CM000670.1:g.19809341C= GRCh37
NC_000008.9:g.19853621C= NCBI36
NG_008855.1:g.17760C=
NG_008855.2:g.55114C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.311C= MANE Select ENSP00000497642.1:p.Pro104=
ENST00000311322.8:c.311C= ENSP00000309757.6:p.Pro104=
ENST00000520959.5:c.83C= ENSP00000428496.1:p.Pro28=
ENST00000522701.5:c.311C= ENSP00000428557.1:p.Pro104=
ENST00000524029.5:c.311C= ENSP00000428237.1:p.Pro104=
NM_000237.2:c.311C= NP_000228.1:p.Pro104=
NM_000237.3:c.311C= MANE Select NP_000228.1:p.Pro104=