Canonical Allele Identifier: CA477047925

Gene: APOA5

Linked Data

• MyVariant Identifiers: chr11:g.116661438A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790722A>G , CM000673.2:g.116790722A>G	GRCh38
NC_000011.9:g.116661438A>G , CM000673.1:g.116661438A>G	GRCh37
NC_000011.8:g.116166648A>G	NCBI36
NG_015894.1:g.6699T>C
NG_015894.2:g.6699T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.507T>C MANE Select	ENSP00000227665.4:p.Ala169=
ENST00000433069.2:c.507T>C	ENSP00000399701.2:p.Ala169=
ENST00000673688.1:c.591T>C	ENSP00000501141.1:p.Ala197=
ENST00000227665.8:c.507T>C	ENSP00000227665.4:p.Ala169=
ENST00000542499.5:c.507T>C	ENSP00000445002.1:p.Ala169=
NM_001166598.1:c.507T>C	NP_001160070.1:p.Ala169=
NM_052968.4:c.507T>C	NP_443200.2:p.Ala169=
NM_001166598.2:c.507T>C	NP_001160070.1:p.Ala169=
NM_001371904.1:c.507T>C MANE Select	NP_001358833.1:p.Ala169=
NM_052968.5:c.507T>C	NP_443200.2:p.Ala169=