Canonical Allele Identifier: CA2616085780

Gene: APOA5

Linked Data

• gnomAD v4: 11-116790194-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790195dup , CM000673.2:g.116790195dup	GRCh38
NC_000011.9:g.116660911dup , CM000673.1:g.116660911dup	GRCh37
NC_000011.8:g.116166121dup	NCBI36
NG_015894.1:g.7226dup
NG_015894.2:g.7226dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.1034dup MANE Select	ENSP00000227665.4:p.Asp345GlufsTer2
ENST00000433069.2:c.1034dup	ENSP00000399701.2:p.Asp345GlufsTer2
ENST00000673688.1:c.1118dup	ENSP00000501141.1:p.Asp373GlufsTer2
ENST00000227665.8:c.1034dup	ENSP00000227665.4:p.Asp345GlufsTer2
ENST00000542499.5:c.1034dup	ENSP00000445002.1:p.Asp345GlufsTer2
NM_001166598.1:c.1034dup	NP_001160070.1:p.Asp345GlufsTer2
NM_052968.4:c.1034dup	NP_443200.2:p.Asp345GlufsTer2
NM_001166598.2:c.1034dup	NP_001160070.1:p.Asp345GlufsTer2
NM_001371904.1:c.1034dup MANE Select	NP_001358833.1:p.Asp345GlufsTer2
NM_052968.5:c.1034dup	NP_443200.2:p.Asp345GlufsTer2