Canonical Allele Identifier: CA2579105838
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954047A>T , CM000670.2:g.19954047A>T GRCh38
NC_000008.10:g.19811558A>T , CM000670.1:g.19811558A>T GRCh37
NC_000008.9:g.19855838A>T NCBI36
NG_008855.1:g.19977A>T
NG_008855.2:g.57331A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-73A>T MANE Select ENSP00000497642.1:n.542-73A>T
ENST00000311322.8:c.542-73A>T ENSP00000309757.6:n.542-73A>T
ENST00000520959.5:c.314-73A>T ENSP00000428496.1:n.314-73A>T
NM_000237.2:c.542-73A>T NP_000228.1:n.542-73A>T
NM_000237.3:c.542-73A>T MANE Select NP_000228.1:n.542-73A>T
Search 100 bp 5'
Search 100 bp 3'