Canonical Allele Identifier: CA2002740618

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790636_116790650delinsAGGCTCTCGGCGTAT , CM000673.2:g.116790636_116790650delinsAGGCTCTCGGCGTAT	GRCh38
NC_000011.9:g.116661352_116661366delinsAGGCTCTCGGCGTAT , CM000673.1:g.116661352_116661366delinsAGGCTCTCGGCGTAT	GRCh37
NC_000011.8:g.116166562_116166576delinsAGGCTCTCGGCGTAT	NCBI36
NG_015894.1:g.6771_6785delinsATACGCCGAGAGCCT
NG_015894.2:g.6771_6785delinsATACGCCGAGAGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.579_593delinsATACGCCGAGAGCCT MANE Select	ENSP00000227665.4:p.Pro193=
ENST00000433069.2:c.579_593delinsATACGCCGAGAGCCT	ENSP00000399701.2:p.Pro193=
ENST00000673688.1:c.663_677delinsATACGCCGAGAGCCT	ENSP00000501141.1:p.Pro221=
ENST00000227665.8:c.579_593delinsATACGCCGAGAGCCT	ENSP00000227665.4:p.Pro193=
ENST00000542499.5:c.579_593delinsATACGCCGAGAGCCT	ENSP00000445002.1:p.Pro193=
NM_001166598.1:c.579_593delinsATACGCCGAGAGCCT	NP_001160070.1:p.Pro193=
NM_052968.4:c.579_593delinsATACGCCGAGAGCCT	NP_443200.2:p.Pro193=
NM_001166598.2:c.579_593delinsATACGCCGAGAGCCT	NP_001160070.1:p.Pro193=
NM_001371904.1:c.579_593delinsATACGCCGAGAGCCT MANE Select	NP_001358833.1:p.Pro193=
NM_052968.5:c.579_593delinsATACGCCGAGAGCCT	NP_443200.2:p.Pro193=