Canonical Allele Identifier: CA477047762

Gene: APOA5

Linked Data

• gnomAD v4: 11-116790665-T-C
• MyVariant Identifiers: chr11:g.116661381T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790665T>C , CM000673.2:g.116790665T>C	GRCh38
NC_000011.9:g.116661381T>C , CM000673.1:g.116661381T>C	GRCh37
NC_000011.8:g.116166591T>C	NCBI36
NG_015894.1:g.6756A>G
NG_015894.2:g.6756A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.564A>G MANE Select	ENSP00000227665.4:p.Lys188=
ENST00000433069.2:c.564A>G	ENSP00000399701.2:p.Lys188=
ENST00000673688.1:c.648A>G	ENSP00000501141.1:p.Lys216=
ENST00000227665.8:c.564A>G	ENSP00000227665.4:p.Lys188=
ENST00000542499.5:c.564A>G	ENSP00000445002.1:p.Lys188=
NM_001166598.1:c.564A>G	NP_001160070.1:p.Lys188=
NM_052968.4:c.564A>G	NP_443200.2:p.Lys188=
NM_001166598.2:c.564A>G	NP_001160070.1:p.Lys188=
NM_001371904.1:c.564A>G MANE Select	NP_001358833.1:p.Lys188=
NM_052968.5:c.564A>G	NP_443200.2:p.Lys188=