Canonical Allele Identifier: CA6289079
Gene: APOA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1284499
ClinVar RCV Id: RCV001699735 RCV001726630
dbSNP Id: rs368739905
ExAC: 11:116661511 T / C
gnomAD v2: 11-116661511-T-C
gnomAD v3: 11-116790795-T-C
gnomAD v4: 11-116790795-T-C
MyVariant Identifiers: chr11:g.116661511T>C (hg19) chr11:g.116790795T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790795T>C , CM000673.2:g.116790795T>C GRCh38
NC_000011.9:g.116661511T>C , CM000673.1:g.116661511T>C GRCh37
NC_000011.8:g.116166721T>C NCBI36
NG_015894.1:g.6626A>G
NG_015894.2:g.6626A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.434A>G MANE Select ENSP00000227665.4:p.Gln145Arg
ENST00000433069.2:c.434A>G ENSP00000399701.2:p.Gln145Arg
ENST00000673688.1:c.518A>G ENSP00000501141.1:p.Gln173Arg
ENST00000227665.8:c.434A>G ENSP00000227665.4:p.Gln145Arg
ENST00000433069.1:c.434A>G ENSP00000399701.1:p.Gln145Arg
ENST00000542499.5:c.434A>G ENSP00000445002.1:p.Gln145Arg
NM_001166598.1:c.434A>G NP_001160070.1:p.Gln145Arg
NM_052968.4:c.434A>G NP_443200.2:p.Gln145Arg
NM_001166598.2:c.434A>G NP_001160070.1:p.Gln145Arg
NM_001371904.1:c.434A>G MANE Select NP_001358833.1:p.Gln145Arg
NM_052968.5:c.434A>G NP_443200.2:p.Gln145Arg
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