Canonical Allele Identifier: CA1769097160
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951596T= , CM000670.2:g.19951596T= GRCh38
NC_000008.10:g.19809107T= , CM000670.1:g.19809107T= GRCh37
NC_000008.9:g.19853387T= NCBI36
NG_008855.1:g.17526T=
NG_008855.2:g.54880T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-173T= MANE Select ENSP00000497642.1:n.250-173T=
ENST00000311322.8:c.250-173T= ENSP00000309757.6:n.250-173T=
ENST00000520959.5:c.22-173T= ENSP00000428496.1:n.22-173T=
ENST00000521994.1:n.435-101T=
ENST00000522701.5:c.250-173T= ENSP00000428557.1:n.250-173T=
ENST00000524029.5:c.250-173T= ENSP00000428237.1:n.250-173T=
NM_000237.2:c.250-173T= NP_000228.1:n.250-173T=
NM_000237.3:c.250-173T= MANE Select NP_000228.1:n.250-173T=