Canonical Allele Identifier: CA2574986415

Gene: APOA5

Linked Data

• gnomAD v4: 11-116791159-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791159A>C , CM000673.2:g.116791159A>C	GRCh38
NC_000011.9:g.116661875A>C , CM000673.1:g.116661875A>C	GRCh37
NC_000011.8:g.116167085A>C	NCBI36
NG_015894.1:g.6262T>G
NG_015894.2:g.6262T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-92T>G MANE Select	ENSP00000227665.4:n.162-92T>G
ENST00000433069.2:c.162-92T>G	ENSP00000399701.2:n.162-92T>G
ENST00000673688.1:c.162-8T>G	ENSP00000501141.1:n.162-8T>G
ENST00000227665.8:c.162-92T>G	ENSP00000227665.4:n.162-92T>G
ENST00000433069.1:c.162-92T>G	ENSP00000399701.1:n.162-92T>G
ENST00000542499.5:c.162-92T>G	ENSP00000445002.1:n.162-92T>G
NM_001166598.1:c.162-92T>G	NP_001160070.1:n.162-92T>G
NM_052968.4:c.162-92T>G	NP_443200.2:n.162-92T>G
NM_001166598.2:c.162-92T>G	NP_001160070.1:n.162-92T>G
NM_001371904.1:c.162-92T>G MANE Select	NP_001358833.1:n.162-92T>G
NM_052968.5:c.162-92T>G	NP_443200.2:n.162-92T>G