Canonical Allele Identifier: CA229336987
Gene: APOA5 HGNC NCBI

Linked Data

dbSNP Id: rs34089864

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790052G>A , CM000673.2:g.116790052G>A GRCh38
NC_000011.9:g.116660768G>A , CM000673.1:g.116660768G>A GRCh37
NC_000011.8:g.116165978G>A NCBI36
NG_015894.1:g.7369C>T
NG_015894.2:g.7369C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227665.9:c.*76C>T MANE Select ENSP00000227665.4:p.=
ENST00000433069.2:c.*76C>T ENSP00000399701.2:p.=
ENST00000227665.8:c.*76C>T ENSP00000227665.4:p.=
ENST00000542499.5:c.*76C>T ENSP00000445002.1:p.=
NM_001166598.1:c.*76C>T NP_001160070.1:p.=
NM_052968.4:c.*76C>T NP_443200.2:p.=
NM_001166598.2:c.*76C>T NP_001160070.1:p.=
NM_001371904.1:c.*76C>T MANE Select NP_001358833.1:p.=
NM_052968.5:c.*76C>T NP_443200.2:p.=