Canonical Allele Identifier: CA173376193
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs996292536
MyVariant Identifiers: chr8:g.19809055T>A (hg19) chr8:g.19951544T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951544T>A , CM000670.2:g.19951544T>A GRCh38
NC_000008.10:g.19809055T>A , CM000670.1:g.19809055T>A GRCh37
NC_000008.9:g.19853335T>A NCBI36
NG_008855.1:g.17474T>A
NG_008855.2:g.54828T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-225T>A MANE Select ENSP00000497642.1:n.250-225T>A
ENST00000311322.8:c.250-225T>A ENSP00000309757.6:n.250-225T>A
ENST00000520959.5:c.22-225T>A ENSP00000428496.1:n.22-225T>A
ENST00000521994.1:n.435-153T>A
ENST00000522701.5:c.250-225T>A ENSP00000428557.1:n.250-225T>A
ENST00000524029.5:c.250-225T>A ENSP00000428237.1:n.250-225T>A
NM_000237.2:c.250-225T>A NP_000228.1:n.250-225T>A
NM_000237.3:c.250-225T>A MANE Select NP_000228.1:n.250-225T>A
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