Canonical Allele Identifier: CA2616086736

Gene: APOA5

Linked Data

• gnomAD v4: 11-116791108-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791110_116791111del , CM000673.2:g.116791110_116791111del	GRCh38
NC_000011.9:g.116661826_116661827del , CM000673.1:g.116661826_116661827del	GRCh37
NC_000011.8:g.116167036_116167037del	NCBI36
NG_015894.1:g.6311_6312del
NG_015894.2:g.6311_6312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-43_162-42del MANE Select	ENSP00000227665.4:n.162-43_162-42del
ENST00000433069.2:c.162-43_162-42del	ENSP00000399701.2:n.162-43_162-42del
ENST00000673688.1:c.203_204del	ENSP00000501141.1:p.Glu68GlyfsTer2
ENST00000227665.8:c.162-43_162-42del	ENSP00000227665.4:n.162-43_162-42del
ENST00000433069.1:c.162-43_162-42del	ENSP00000399701.1:n.162-43_162-42del
ENST00000542499.5:c.162-43_162-42del	ENSP00000445002.1:n.162-43_162-42del
NM_001166598.1:c.162-43_162-42del	NP_001160070.1:n.162-43_162-42del
NM_052968.4:c.162-43_162-42del	NP_443200.2:n.162-43_162-42del
NM_001166598.2:c.162-43_162-42del	NP_001160070.1:n.162-43_162-42del
NM_001371904.1:c.162-43_162-42del MANE Select	NP_001358833.1:n.162-43_162-42del
NM_052968.5:c.162-43_162-42del	NP_443200.2:n.162-43_162-42del