Canonical Allele Identifier: CA942583341

Gene: APOA5

Linked Data

• dbSNP Id: rs1941002995
• gnomAD v3: 11-116791126-T-A
• gnomAD v4: 11-116791126-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791126T>A , CM000673.2:g.116791126T>A	GRCh38
NC_000011.9:g.116661842T>A , CM000673.1:g.116661842T>A	GRCh37
NC_000011.8:g.116167052T>A	NCBI36
NG_015894.1:g.6295A>T
NG_015894.2:g.6295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-59A>T MANE Select	ENSP00000227665.4:n.162-59A>T
ENST00000433069.2:c.162-59A>T	ENSP00000399701.2:n.162-59A>T
ENST00000673688.1:c.187A>T	ENSP00000501141.1:p.Thr63Ser
ENST00000227665.8:c.162-59A>T	ENSP00000227665.4:n.162-59A>T
ENST00000433069.1:c.162-59A>T	ENSP00000399701.1:n.162-59A>T
ENST00000542499.5:c.162-59A>T	ENSP00000445002.1:n.162-59A>T
NM_001166598.1:c.162-59A>T	NP_001160070.1:n.162-59A>T
NM_052968.4:c.162-59A>T	NP_443200.2:n.162-59A>T
NM_001166598.2:c.162-59A>T	NP_001160070.1:n.162-59A>T
NM_001371904.1:c.162-59A>T MANE Select	NP_001358833.1:n.162-59A>T
NM_052968.5:c.162-59A>T	NP_443200.2:n.162-59A>T