Canonical Allele Identifier: CA229337863
Gene: APOA5 HGNC NCBI

Linked Data

dbSNP Id: rs34543602

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790690A>T , CM000673.2:g.116790690A>T GRCh38
NC_000011.9:g.116661406A>T , CM000673.1:g.116661406A>T GRCh37
NC_000011.8:g.116166616A>T NCBI36
NG_015894.1:g.6731T>A
NG_015894.2:g.6731T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.539T>A MANE Select ENSP00000227665.4:p.Val180Glu
ENST00000433069.2:c.539T>A ENSP00000399701.2:p.Val180Glu
ENST00000673688.1:c.623T>A ENSP00000501141.1:p.Val208Glu
ENST00000227665.8:c.539T>A ENSP00000227665.4:p.Val180Glu
ENST00000542499.5:c.539T>A ENSP00000445002.1:p.Val180Glu
NM_001166598.1:c.539T>A NP_001160070.1:p.Val180Glu
NM_052968.4:c.539T>A NP_443200.2:p.Val180Glu
NM_001166598.2:c.539T>A NP_001160070.1:p.Val180Glu
NM_001371904.1:c.539T>A MANE Select NP_001358833.1:p.Val180Glu
NM_052968.5:c.539T>A NP_443200.2:p.Val180Glu