Canonical Allele Identifier: CA2695215435

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790782delinsGAG , CM000673.2:g.116790782delinsGAG	GRCh38
NC_000011.9:g.116661498delinsGAG , CM000673.1:g.116661498delinsGAG	GRCh37
NC_000011.8:g.116166708delinsGAG	NCBI36
NG_015894.1:g.6639delinsCTC
NG_015894.2:g.6639delinsCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.447delinsCTC MANE Select	ENSP00000227665.4:p.Glu149AspfsTer?
ENST00000433069.2:c.447delinsCTC	ENSP00000399701.2:p.Glu149AspfsTer?
ENST00000673688.1:c.531delinsCTC	ENSP00000501141.1:p.Glu177AspfsTer?
ENST00000227665.8:c.447delinsCTC	ENSP00000227665.4:p.Glu149AspfsTer?
ENST00000433069.1:c.447delinsCTC	ENSP00000399701.1:p.Glu149AspfsTer?
ENST00000542499.5:c.447delinsCTC	ENSP00000445002.1:p.Glu149AspfsTer?
NM_001166598.1:c.447delinsCTC	NP_001160070.1:p.Glu149AspfsTer?
NM_052968.4:c.447delinsCTC	NP_443200.2:p.Glu149AspfsTer?
NM_001166598.2:c.447delinsCTC	NP_001160070.1:p.Glu149AspfsTer?
NM_001371904.1:c.447delinsCTC MANE Select	NP_001358833.1:p.Glu149AspfsTer?
NM_052968.5:c.447delinsCTC	NP_443200.2:p.Glu149AspfsTer?