Canonical Allele Identifier: CA1769096933
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951495T= , CM000670.2:g.19951495T= GRCh38
NC_000008.10:g.19809006T= , CM000670.1:g.19809006T= GRCh37
NC_000008.9:g.19853286T= NCBI36
NG_008855.1:g.17425T=
NG_008855.2:g.54779T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-274T= MANE Select ENSP00000497642.1:n.250-274T=
ENST00000311322.8:c.250-274T= ENSP00000309757.6:n.250-274T=
ENST00000520959.5:c.22-274T= ENSP00000428496.1:n.22-274T=
ENST00000521994.1:n.435-202T=
ENST00000522701.5:c.250-274T= ENSP00000428557.1:n.250-274T=
ENST00000524029.5:c.250-274T= ENSP00000428237.1:n.250-274T=
NM_000237.2:c.250-274T= NP_000228.1:n.250-274T=
NM_000237.3:c.250-274T= MANE Select NP_000228.1:n.250-274T=
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