Canonical Allele Identifier: CA6289120

Gene: APOA5

Linked Data

• dbSNP Id: rs764339074
• ExAC: 11:116661803 T / C
• gnomAD v2: 11-116661803-T-C
• MyVariant Identifiers: chr11:g.116661803T>C (hg19) ; chr11:g.116791087T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791087T>C , CM000673.2:g.116791087T>C	GRCh38
NC_000011.9:g.116661803T>C , CM000673.1:g.116661803T>C	GRCh37
NC_000011.8:g.116167013T>C	NCBI36
NG_015894.1:g.6334A>G
NG_015894.2:g.6334A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-20A>G MANE Select	ENSP00000227665.4:n.162-20A>G
ENST00000433069.2:c.162-20A>G	ENSP00000399701.2:n.162-20A>G
ENST00000673688.1:c.226A>G	ENSP00000501141.1:p.Ile76Val
ENST00000227665.8:c.162-20A>G	ENSP00000227665.4:n.162-20A>G
ENST00000433069.1:c.162-20A>G	ENSP00000399701.1:n.162-20A>G
ENST00000542499.5:c.162-20A>G	ENSP00000445002.1:n.162-20A>G
NM_001166598.1:c.162-20A>G	NP_001160070.1:n.162-20A>G
NM_052968.4:c.162-20A>G	NP_443200.2:n.162-20A>G
NM_001166598.2:c.162-20A>G	NP_001160070.1:n.162-20A>G
NM_001371904.1:c.162-20A>G MANE Select	NP_001358833.1:n.162-20A>G
NM_052968.5:c.162-20A>G	NP_443200.2:n.162-20A>G