Canonical Allele Identifier: CA370468295
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954141A>C , CM000670.2:g.19954141A>C GRCh38
NC_000008.10:g.19811652A>C , CM000670.1:g.19811652A>C GRCh37
NC_000008.9:g.19855932A>C NCBI36
NG_008855.1:g.20071A>C
NG_008855.2:g.57425A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.563A>C MANE Select ENSP00000497642.1:p.Asn188Thr
ENST00000311322.8:c.563A>C ENSP00000309757.6:p.Asn188Thr
ENST00000520959.5:c.335A>C ENSP00000428496.1:p.Asn112Thr
NM_000237.2:c.563A>C NP_000228.1:p.Asn188Thr
NM_000237.3:c.563A>C MANE Select NP_000228.1:p.Asn188Thr