Canonical Allele Identifier: CA2002740638
Gene: APOA5 HGNC NCBI

Linked Data

dbSNP Id: rs1940989285

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790640_116790641insGGAAGAG , CM000673.2:g.116790640_116790641insGGAAGAG GRCh38
NC_000011.9:g.116661356_116661357insGGAAGAG , CM000673.1:g.116661356_116661357insGGAAGAG GRCh37
NC_000011.8:g.116166566_116166567insGGAAGAG NCBI36
NG_015894.1:g.6780_6781insCTCTTCC
NG_015894.2:g.6780_6781insCTCTTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.588_589insCTCTTCC MANE Select ENSP00000227665.4:p.Ser197LeufsTer?
ENST00000433069.2:c.588_589insCTCTTCC ENSP00000399701.2:p.Ser197LeufsTer?
ENST00000673688.1:c.672_673insCTCTTCC ENSP00000501141.1:p.Ser225LeufsTer?
ENST00000227665.8:c.588_589insCTCTTCC ENSP00000227665.4:p.Ser197LeufsTer?
ENST00000542499.5:c.588_589insCTCTTCC ENSP00000445002.1:p.Ser197LeufsTer?
NM_001166598.1:c.588_589insCTCTTCC NP_001160070.1:p.Ser197LeufsTer?
NM_052968.4:c.588_589insCTCTTCC NP_443200.2:p.Ser197LeufsTer?
NM_001166598.2:c.588_589insCTCTTCC NP_001160070.1:p.Ser197LeufsTer?
NM_001371904.1:c.588_589insCTCTTCC MANE Select NP_001358833.1:p.Ser197LeufsTer?
NM_052968.5:c.588_589insCTCTTCC NP_443200.2:p.Ser197LeufsTer?