Canonical Allele Identifier: CA6289114

Gene: APOA5

Linked Data

• dbSNP Id: rs770971777
• ExAC: 11:116661750 G / A
• gnomAD v2: 11-116661750-G-A
• gnomAD v3: 11-116791034-G-A
• gnomAD v4: 11-116791034-G-A
• MyVariant Identifiers: chr11:g.116661750G>A (hg19) ; chr11:g.116791034G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791034G>A , CM000673.2:g.116791034G>A	GRCh38
NC_000011.9:g.116661750G>A , CM000673.1:g.116661750G>A	GRCh37
NC_000011.8:g.116166960G>A	NCBI36
NG_015894.1:g.6387C>T
NG_015894.2:g.6387C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.195C>T MANE Select	ENSP00000227665.4:p.Asn65=
ENST00000433069.2:c.195C>T	ENSP00000399701.2:p.Asn65=
ENST00000673688.1:c.279C>T	ENSP00000501141.1:p.Asn93=
ENST00000227665.8:c.195C>T	ENSP00000227665.4:p.Asn65=
ENST00000433069.1:c.195C>T	ENSP00000399701.1:p.Asn65=
ENST00000542499.5:c.195C>T	ENSP00000445002.1:p.Asn65=
NM_001166598.1:c.195C>T	NP_001160070.1:p.Asn65=
NM_052968.4:c.195C>T	NP_443200.2:p.Asn65=
NM_001166598.2:c.195C>T	NP_001160070.1:p.Asn65=
NM_001371904.1:c.195C>T MANE Select	NP_001358833.1:p.Asn65=
NM_052968.5:c.195C>T	NP_443200.2:p.Asn65=