Canonical Allele Identifier: CA2002741382

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116791144_116791146delinsCTG , CM000673.2:g.116791144_116791146delinsCTG	GRCh38
NC_000011.9:g.116661860_116661862delinsCTG , CM000673.1:g.116661860_116661862delinsCTG	GRCh37
NC_000011.8:g.116167070_116167072delinsCTG	NCBI36
NG_015894.1:g.6275_6277delinsCAG
NG_015894.2:g.6275_6277delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.162-79_162-77delinsCAG MANE Select	ENSP00000227665.4:n.162-79_162-77delinsCAG
ENST00000433069.2:c.162-79_162-77delinsCAG	ENSP00000399701.2:n.162-79_162-77delinsCAG
ENST00000673688.1:c.167_169delinsCAG	ENSP00000501141.1:p.Ser56=
ENST00000227665.8:c.162-79_162-77delinsCAG	ENSP00000227665.4:n.162-79_162-77delinsCAG
ENST00000433069.1:c.162-79_162-77delinsCAG	ENSP00000399701.1:n.162-79_162-77delinsCAG
ENST00000542499.5:c.162-79_162-77delinsCAG	ENSP00000445002.1:n.162-79_162-77delinsCAG
NM_001166598.1:c.162-79_162-77delinsCAG	NP_001160070.1:n.162-79_162-77delinsCAG
NM_052968.4:c.162-79_162-77delinsCAG	NP_443200.2:n.162-79_162-77delinsCAG
NM_001166598.2:c.162-79_162-77delinsCAG	NP_001160070.1:n.162-79_162-77delinsCAG
NM_001371904.1:c.162-79_162-77delinsCAG MANE Select	NP_001358833.1:n.162-79_162-77delinsCAG
NM_052968.5:c.162-79_162-77delinsCAG	NP_443200.2:n.162-79_162-77delinsCAG