Canonical Allele Identifier: CA6289124

Gene: APOA5

Linked Data

• ClinVar Variation Id: 1297445
• ClinVar RCV Id: RCV001723230
• dbSNP Id: rs2072560
• ExAC: 11:116661826 T / C
• gnomAD v2: 11-116661826-T-C
• gnomAD v3: 11-116791110-T-C
• gnomAD v4: 11-116791110-T-C
• MyVariant Identifiers: chr11:g.116661826T>C (hg19) ; chr11:g.116791110T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791110T>C , CM000673.2:g.116791110T>C	GRCh38
NC_000011.9:g.116661826T>C , CM000673.1:g.116661826T>C	GRCh37
NC_000011.8:g.116167036T>C	NCBI36
NG_015894.1:g.6311A>G
NG_015894.2:g.6311A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-43A>G MANE Select	ENSP00000227665.4:n.162-43A>G
ENST00000433069.2:c.162-43A>G	ENSP00000399701.2:n.162-43A>G
ENST00000673688.1:c.203A>G	ENSP00000501141.1:p.Glu68Gly
ENST00000227665.8:c.162-43A>G	ENSP00000227665.4:n.162-43A>G
ENST00000433069.1:c.162-43A>G	ENSP00000399701.1:n.162-43A>G
ENST00000542499.5:c.162-43A>G	ENSP00000445002.1:n.162-43A>G
NM_001166598.1:c.162-43A>G	NP_001160070.1:n.162-43A>G
NM_052968.4:c.162-43A>G	NP_443200.2:n.162-43A>G
NM_001166598.2:c.162-43A>G	NP_001160070.1:n.162-43A>G
NM_001371904.1:c.162-43A>G MANE Select	NP_001358833.1:n.162-43A>G
NM_052968.5:c.162-43A>G	NP_443200.2:n.162-43A>G