Canonical Allele Identifier: CA382740482
Gene: APOA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116791059T>G , CM000673.2:g.116791059T>G GRCh38
NC_000011.9:g.116661775T>G , CM000673.1:g.116661775T>G GRCh37
NC_000011.8:g.116166985T>G NCBI36
NG_015894.1:g.6362A>C
NG_015894.2:g.6362A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227665.9:c.170A>C MANE Select ENSP00000227665.4:p.Lys57Thr
ENST00000433069.2:c.170A>C ENSP00000399701.2:p.Lys57Thr
ENST00000673688.1:c.254A>C ENSP00000501141.1:p.Lys85Thr
ENST00000227665.8:c.170A>C ENSP00000227665.4:p.Lys57Thr
ENST00000433069.1:c.170A>C ENSP00000399701.1:p.Lys57Thr
ENST00000542499.5:c.170A>C ENSP00000445002.1:p.Lys57Thr
NM_001166598.1:c.170A>C NP_001160070.1:p.Lys57Thr
NM_052968.4:c.170A>C NP_443200.2:p.Lys57Thr
NM_001166598.2:c.170A>C NP_001160070.1:p.Lys57Thr
NM_001371904.1:c.170A>C MANE Select NP_001358833.1:p.Lys57Thr
NM_052968.5:c.170A>C NP_443200.2:p.Lys57Thr