Canonical Allele Identifier: CA2002740668

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790646_116790650delinsCGTAT , CM000673.2:g.116790646_116790650delinsCGTAT	GRCh38
NC_000011.9:g.116661362_116661366delinsCGTAT , CM000673.1:g.116661362_116661366delinsCGTAT	GRCh37
NC_000011.8:g.116166572_116166576delinsCGTAT	NCBI36
NG_015894.1:g.6771_6775delinsATACG
NG_015894.2:g.6771_6775delinsATACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.579_583delinsATACG MANE Select	ENSP00000227665.4:p.Pro193=
ENST00000433069.2:c.579_583delinsATACG	ENSP00000399701.2:p.Pro193=
ENST00000673688.1:c.663_667delinsATACG	ENSP00000501141.1:p.Pro221=
ENST00000227665.8:c.579_583delinsATACG	ENSP00000227665.4:p.Pro193=
ENST00000542499.5:c.579_583delinsATACG	ENSP00000445002.1:p.Pro193=
NM_001166598.1:c.579_583delinsATACG	NP_001160070.1:p.Pro193=
NM_052968.4:c.579_583delinsATACG	NP_443200.2:p.Pro193=
NM_001166598.2:c.579_583delinsATACG	NP_001160070.1:p.Pro193=
NM_001371904.1:c.579_583delinsATACG MANE Select	NP_001358833.1:p.Pro193=
NM_052968.5:c.579_583delinsATACG	NP_443200.2:p.Pro193=