Canonical Allele Identifier: CA2002740731

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790675_116790676delinsCC , CM000673.2:g.116790675_116790676delinsCC	GRCh38
NC_000011.9:g.116661391_116661392delinsCC , CM000673.1:g.116661391_116661392delinsCC	GRCh37
NC_000011.8:g.116166601_116166602delinsCC	NCBI36
NG_015894.1:g.6745_6746delinsGG
NG_015894.2:g.6745_6746delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.553_554delinsGG MANE Select	ENSP00000227665.4:p.Gly185=
ENST00000433069.2:c.553_554delinsGG	ENSP00000399701.2:p.Gly185=
ENST00000673688.1:c.637_638delinsGG	ENSP00000501141.1:p.Gly213=
ENST00000227665.8:c.553_554delinsGG	ENSP00000227665.4:p.Gly185=
ENST00000542499.5:c.553_554delinsGG	ENSP00000445002.1:p.Gly185=
NM_001166598.1:c.553_554delinsGG	NP_001160070.1:p.Gly185=
NM_052968.4:c.553_554delinsGG	NP_443200.2:p.Gly185=
NM_001166598.2:c.553_554delinsGG	NP_001160070.1:p.Gly185=
NM_001371904.1:c.553_554delinsGG MANE Select	NP_001358833.1:p.Gly185=
NM_052968.5:c.553_554delinsGG	NP_443200.2:p.Gly185=