Canonical Allele Identifier: CA1769106647
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957585A>C , CM000670.2:g.19957585A>C GRCh38
NC_000008.10:g.19815096A>C , CM000670.1:g.19815096A>C GRCh37
NC_000008.9:g.19859376A>C NCBI36
NG_008855.1:g.23515A>C
NG_008855.2:g.60869A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1502A>C MANE Select ENSP00000497642.1:p.=
ENST00000650478.1:n.79+1502A>C ENSP00000497560.1:p.=
ENST00000311322.8:c.1018+1502A>C ENSP00000309757.6:p.=
NM_000237.2:c.1018+1502A>C NP_000228.1:p.=
NM_000237.3:c.1018+1502A>C MANE Select NP_000228.1:p.=