Canonical Allele Identifier: CA382740562

Gene: APOA5

Linked Data

• MyVariant Identifiers: chr11:g.116661785T>A (hg19) ; chr11:g.116791069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791069T>A , CM000673.2:g.116791069T>A	GRCh38
NC_000011.9:g.116661785T>A , CM000673.1:g.116661785T>A	GRCh37
NC_000011.8:g.116166995T>A	NCBI36
NG_015894.1:g.6352A>T
NG_015894.2:g.6352A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-2A>T MANE Select	ENSP00000227665.4:n.162-2A>T
ENST00000433069.2:c.162-2A>T	ENSP00000399701.2:n.162-2A>T
ENST00000673688.1:c.244A>T	ENSP00000501141.1:p.Arg82Trp
ENST00000227665.8:c.162-2A>T	ENSP00000227665.4:n.162-2A>T
ENST00000433069.1:c.162-2A>T	ENSP00000399701.1:n.162-2A>T
ENST00000542499.5:c.162-2A>T	ENSP00000445002.1:n.162-2A>T
NM_001166598.1:c.162-2A>T	NP_001160070.1:n.162-2A>T
NM_052968.4:c.162-2A>T	NP_443200.2:n.162-2A>T
NM_001166598.2:c.162-2A>T	NP_001160070.1:n.162-2A>T
NM_001371904.1:c.162-2A>T MANE Select	NP_001358833.1:n.162-2A>T
NM_052968.5:c.162-2A>T	NP_443200.2:n.162-2A>T