Canonical Allele Identifier: CA2002739813
Gene: APOA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790113T= , CM000673.2:g.116790113T= GRCh38
NC_000011.9:g.116660829T= , CM000673.1:g.116660829T= GRCh37
NC_000011.8:g.116166039T= NCBI36
NG_015894.1:g.7308A=
NG_015894.2:g.7308A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.*15A= MANE Select ENSP00000227665.4:n.*15A=
ENST00000433069.2:c.*15A= ENSP00000399701.2:n.*15A=
ENST00000673688.1:c.*15A= ENSP00000501141.1:n.*15A=
ENST00000227665.8:c.*15A= ENSP00000227665.4:n.*15A=
ENST00000542499.5:c.*15A= ENSP00000445002.1:n.*15A=
NM_001166598.1:c.*15A= NP_001160070.1:n.*15A=
NM_052968.4:c.*15A= NP_443200.2:n.*15A=
NM_001166598.2:c.*15A= NP_001160070.1:n.*15A=
NM_001371904.1:c.*15A= MANE Select NP_001358833.1:n.*15A=
NM_052968.5:c.*15A= NP_443200.2:n.*15A=