Canonical Allele Identifier: CA382738373
Gene: APOA5 HGNC NCBI

Linked Data

dbSNP Id: rs916656857

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790775G>T , CM000673.2:g.116790775G>T GRCh38
NC_000011.9:g.116661491G>T , CM000673.1:g.116661491G>T GRCh37
NC_000011.8:g.116166701G>T NCBI36
NG_015894.1:g.6646C>A
NG_015894.2:g.6646C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.454C>A MANE Select ENSP00000227665.4:p.Arg152Ser
ENST00000433069.2:c.454C>A ENSP00000399701.2:p.Arg152Ser
ENST00000673688.1:c.538C>A ENSP00000501141.1:p.Arg180Ser
ENST00000227665.8:c.454C>A ENSP00000227665.4:p.Arg152Ser
ENST00000433069.1:c.454C>A ENSP00000399701.1:p.Arg152Ser
ENST00000542499.5:c.454C>A ENSP00000445002.1:p.Arg152Ser
NM_001166598.1:c.454C>A NP_001160070.1:p.Arg152Ser
NM_052968.4:c.454C>A NP_443200.2:p.Arg152Ser
NM_001166598.2:c.454C>A NP_001160070.1:p.Arg152Ser
NM_001371904.1:c.454C>A MANE Select NP_001358833.1:p.Arg152Ser
NM_052968.5:c.454C>A NP_443200.2:p.Arg152Ser