Canonical Allele Identifier: CA601831219

Gene: APOA5

Linked Data

• dbSNP Id: rs1156417726
• gnomAD v2: 11-116661859-A-C
• gnomAD v4: 11-116791143-A-C
• MyVariant Identifiers: chr11:g.116661859A>C (hg19) ; chr11:g.116791143A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791143A>C , CM000673.2:g.116791143A>C	GRCh38
NC_000011.9:g.116661859A>C , CM000673.1:g.116661859A>C	GRCh37
NC_000011.8:g.116167069A>C	NCBI36
NG_015894.1:g.6278T>G
NG_015894.2:g.6278T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-76T>G MANE Select	ENSP00000227665.4:n.162-76T>G
ENST00000433069.2:c.162-76T>G	ENSP00000399701.2:n.162-76T>G
ENST00000673688.1:c.170T>G	ENSP00000501141.1:p.Val57Gly
ENST00000227665.8:c.162-76T>G	ENSP00000227665.4:n.162-76T>G
ENST00000433069.1:c.162-76T>G	ENSP00000399701.1:n.162-76T>G
ENST00000542499.5:c.162-76T>G	ENSP00000445002.1:n.162-76T>G
NM_001166598.1:c.162-76T>G	NP_001160070.1:n.162-76T>G
NM_052968.4:c.162-76T>G	NP_443200.2:n.162-76T>G
NM_001166598.2:c.162-76T>G	NP_001160070.1:n.162-76T>G
NM_001371904.1:c.162-76T>G MANE Select	NP_001358833.1:n.162-76T>G
NM_052968.5:c.162-76T>G	NP_443200.2:n.162-76T>G