Canonical Allele Identifier: CA459719140
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19818424C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960913C>A , CM000670.2:g.19960913C>A GRCh38
NC_000008.10:g.19818424C>A , CM000670.1:g.19818424C>A GRCh37
NC_000008.9:g.19862704C>A NCBI36
NG_008855.1:g.26843C>A
NG_008855.2:g.64197C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1152C>A MANE Select ENSP00000497642.1:p.Ser384=
ENST00000650478.1:c.92C>A ENSP00000497560.1:p.Pro31Gln
ENST00000311322.8:c.1152C>A ENSP00000309757.6:p.Ser384=
NM_000237.2:c.1152C>A NP_000228.1:p.Ser384=
NM_000237.3:c.1152C>A MANE Select NP_000228.1:p.Ser384=
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