Canonical Allele Identifier: CA1769101621
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954008G= , CM000670.2:g.19954008G= GRCh38
NC_000008.10:g.19811519G= , CM000670.1:g.19811519G= GRCh37
NC_000008.9:g.19855799G= NCBI36
NG_008855.1:g.19938G=
NG_008855.2:g.57292G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-112G= MANE Select ENSP00000497642.1:n.542-112G=
ENST00000311322.8:c.542-112G= ENSP00000309757.6:n.542-112G=
ENST00000520959.5:c.314-112G= ENSP00000428496.1:n.314-112G=
NM_000237.2:c.542-112G= NP_000228.1:n.542-112G=
NM_000237.3:c.542-112G= MANE Select NP_000228.1:n.542-112G=
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