Canonical Allele Identifier: CA1202652436

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222670_161222672delinsTAG , CM000663.2:g.161222670_161222672delinsTAG	GRCh38
NC_000001.10:g.161192460_161192462delinsTAG , CM000663.1:g.161192460_161192462delinsTAG	GRCh37
NC_000001.9:g.159459084_159459086delinsTAG	NCBI36
NG_012043.1:g.5957_5959delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.186-150_186-148delinsCTA MANE Select	ENSP00000356969.3:n.186-150_186-148delinsCTA
ENST00000463273.5:c.186-150_186-148delinsCTA	ENSP00000476740.1:n.186-150_186-148delinsCTA
ENST00000463812.1:c.42-150_42-148delinsCTA	ENSP00000476890.1:n.42-150_42-148delinsCTA
ENST00000464492.5:c.285-150_285-148delinsCTA	ENSP00000476911.1:n.285-150_285-148delinsCTA
ENST00000468465.5:c.42-150_42-148delinsCTA	ENSP00000476662.1:n.42-150_42-148delinsCTA
ENST00000469730.2:c.186-150_186-148delinsCTA	ENSP00000476605.1:n.186-150_186-148delinsCTA
ENST00000470459.6:c.186-150_186-148delinsCTA	ENSP00000477031.1:n.186-150_186-148delinsCTA
ENST00000481413.1:n.697-150_697-148delinsCTA
ENST00000481511.5:c.*183-150_*183-148delinsCTA	ENSP00000477054.1:n.*183-150_*183-148delinsCTA
ENST00000491350.1:c.53-150_53-148delinsCTA	ENSP00000477353.1:n.53-150_53-148delinsCTA
NM_001643.1:c.186-150_186-148delinsCTA	NP_001634.1:n.186-150_186-148delinsCTA
NM_001643.2:c.186-150_186-148delinsCTA MANE Select	NP_001634.1:n.186-150_186-148delinsCTA