Canonical Allele Identifier: CA6288946

Gene: APOA5

Linked Data

• dbSNP Id: rs770798013
• ExAC: 11:116660920 G / GCCCACAATCCCTGAATC
• MyVariant Identifiers: chr11:g.116660920_116660921insCCCACAATCCCTGAATC (hg19) ; chr11:g.116790204_116790205insCCCACAATCCCTGAATC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790206_116790207insCACAATCCCTGAATCCC , CM000673.2:g.116790206_116790207insCACAATCCCTGAATCCC	GRCh38
NC_000011.9:g.116660922_116660923insCACAATCCCTGAATCCC , CM000673.1:g.116660922_116660923insCACAATCCCTGAATCCC	GRCh37
NC_000011.8:g.116166132_116166133insCACAATCCCTGAATCCC	NCBI36
NG_015894.1:g.7216_7217insGATTCAGGGATTGTGGG
NG_015894.2:g.7216_7217insGATTCAGGGATTGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.1024_1025insGATTCAGGGATTGTGGG MANE Select	ENSP00000227665.4:p.Ala342GlyfsTer?
ENST00000433069.2:c.1024_1025insGATTCAGGGATTGTGGG	ENSP00000399701.2:p.Ala342GlyfsTer?
ENST00000673688.1:c.1108_1109insGATTCAGGGATTGTGGG	ENSP00000501141.1:p.Ala370GlyfsTer?
ENST00000227665.8:c.1024_1025insGATTCAGGGATTGTGGG	ENSP00000227665.4:p.Ala342GlyfsTer?
ENST00000542499.5:c.1024_1025insGATTCAGGGATTGTGGG	ENSP00000445002.1:p.Ala342GlyfsTer?
NM_001166598.1:c.1024_1025insGATTCAGGGATTGTGGG	NP_001160070.1:p.Ala342GlyfsTer?
NM_052968.4:c.1024_1025insGATTCAGGGATTGTGGG	NP_443200.2:p.Ala342GlyfsTer?
NM_001166598.2:c.1024_1025insGATTCAGGGATTGTGGG	NP_001160070.1:p.Ala342GlyfsTer?
NM_001371904.1:c.1024_1025insGATTCAGGGATTGTGGG MANE Select	NP_001358833.1:p.Ala342GlyfsTer?
NM_052968.5:c.1024_1025insGATTCAGGGATTGTGGG	NP_443200.2:p.Ala342GlyfsTer?