Canonical Allele Identifier: CA459719166
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19818463A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960952A>C , CM000670.2:g.19960952A>C GRCh38
NC_000008.10:g.19818463A>C , CM000670.1:g.19818463A>C GRCh37
NC_000008.9:g.19862743A>C NCBI36
NG_008855.1:g.26882A>C
NG_008855.2:g.64236A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1191A>C MANE Select ENSP00000497642.1:p.Val397=
ENST00000650478.1:c.131A>C ENSP00000497560.1:n.131A>C
ENST00000311322.8:c.1191A>C ENSP00000309757.6:p.Val397=
NM_000237.2:c.1191A>C NP_000228.1:p.Val397=
NM_000237.3:c.1191A>C MANE Select NP_000228.1:p.Val397=