Canonical Allele Identifier: CA918975684

Gene: APOA5

Linked Data

• dbSNP Id: rs1591312974

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790676delinsGT , CM000673.2:g.116790676delinsGT	GRCh38
NC_000011.9:g.116661392delinsGT , CM000673.1:g.116661392delinsGT	GRCh37
NC_000011.8:g.116166602delinsGT	NCBI36
NG_015894.1:g.6745delinsAC
NG_015894.2:g.6745delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.553delinsAC MANE Select	ENSP00000227665.4:p.Gly185ThrfsTer?
ENST00000433069.2:c.553delinsAC	ENSP00000399701.2:p.Gly185ThrfsTer?
ENST00000673688.1:c.637delinsAC	ENSP00000501141.1:p.Gly213ThrfsTer?
ENST00000227665.8:c.553delinsAC	ENSP00000227665.4:p.Gly185ThrfsTer?
ENST00000542499.5:c.553delinsAC	ENSP00000445002.1:p.Gly185ThrfsTer?
NM_001166598.1:c.553delinsAC	NP_001160070.1:p.Gly185ThrfsTer?
NM_052968.4:c.553delinsAC	NP_443200.2:p.Gly185ThrfsTer?
NM_001166598.2:c.553delinsAC	NP_001160070.1:p.Gly185ThrfsTer?
NM_001371904.1:c.553delinsAC MANE Select	NP_001358833.1:p.Gly185ThrfsTer?
NM_052968.5:c.553delinsAC	NP_443200.2:p.Gly185ThrfsTer?