Canonical Allele Identifier: CA2616086277

Gene: APOA5

Linked Data

• gnomAD v4: 11-116790638-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790642_116790643del , CM000673.2:g.116790642_116790643del	GRCh38
NC_000011.9:g.116661358_116661359del , CM000673.1:g.116661358_116661359del	GRCh37
NC_000011.8:g.116166568_116166569del	NCBI36
NG_015894.1:g.6781_6782del
NG_015894.2:g.6781_6782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.589_590del MANE Select	ENSP00000227665.4:p.Ser197ProfsTer?
ENST00000433069.2:c.589_590del	ENSP00000399701.2:p.Ser197ProfsTer?
ENST00000673688.1:c.673_674del	ENSP00000501141.1:p.Ser225ProfsTer?
ENST00000227665.8:c.589_590del	ENSP00000227665.4:p.Ser197ProfsTer?
ENST00000542499.5:c.589_590del	ENSP00000445002.1:p.Ser197ProfsTer?
NM_001166598.1:c.589_590del	NP_001160070.1:p.Ser197ProfsTer?
NM_052968.4:c.589_590del	NP_443200.2:p.Ser197ProfsTer?
NM_001166598.2:c.589_590del	NP_001160070.1:p.Ser197ProfsTer?
NM_001371904.1:c.589_590del MANE Select	NP_001358833.1:p.Ser197ProfsTer?
NM_052968.5:c.589_590del	NP_443200.2:p.Ser197ProfsTer?