Canonical Allele Identifier: CA6288931
Gene: APOA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1293389
ClinVar RCV Id: RCV001717563
dbSNP Id: rs619054

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790097G>A , CM000673.2:g.116790097G>A GRCh38
NC_000011.9:g.116660813G>A , CM000673.1:g.116660813G>A GRCh37
NC_000011.8:g.116166023G>A NCBI36
NG_015894.1:g.7324C>T
NG_015894.2:g.7324C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227665.9:c.*31C>T MANE Select ENSP00000227665.4:n.*31C>T
ENST00000433069.2:c.*31C>T ENSP00000399701.2:n.*31C>T
ENST00000673688.1:c.*31C>T ENSP00000501141.1:n.*31C>T
ENST00000227665.8:c.*31C>T ENSP00000227665.4:n.*31C>T
ENST00000542499.5:c.*31C>T ENSP00000445002.1:n.*31C>T
NM_001166598.1:c.*31C>T NP_001160070.1:n.*31C>T
NM_052968.4:c.*31C>T NP_443200.2:n.*31C>T
NM_001166598.2:c.*31C>T NP_001160070.1:n.*31C>T
NM_001371904.1:c.*31C>T MANE Select NP_001358833.1:n.*31C>T
NM_052968.5:c.*31C>T NP_443200.2:n.*31C>T