Canonical Allele Identifier: CA2002739753
Gene: APOA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790056G= , CM000673.2:g.116790056G= GRCh38
NC_000011.9:g.116660772G= , CM000673.1:g.116660772G= GRCh37
NC_000011.8:g.116165982G= NCBI36
NG_015894.1:g.7365C=
NG_015894.2:g.7365C=

Transcript Alleles

HGVS Amino-acid change
ENST00000227665.9:c.*72C= MANE Select ENSP00000227665.4:n.*72C=
ENST00000433069.2:c.*72C= ENSP00000399701.2:n.*72C=
ENST00000227665.8:c.*72C= ENSP00000227665.4:n.*72C=
ENST00000542499.5:c.*72C= ENSP00000445002.1:n.*72C=
NM_001166598.1:c.*72C= NP_001160070.1:n.*72C=
NM_052968.4:c.*72C= NP_443200.2:n.*72C=
NM_001166598.2:c.*72C= NP_001160070.1:n.*72C=
NM_001371904.1:c.*72C= MANE Select NP_001358833.1:n.*72C=
NM_052968.5:c.*72C= NP_443200.2:n.*72C=