Canonical Allele Identifier: CA1202652370

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222568_161222578delinsACTGGCAGGGG , CM000663.2:g.161222568_161222578delinsACTGGCAGGGG	GRCh38
NC_000001.10:g.161192358_161192368delinsACTGGCAGGGG , CM000663.1:g.161192358_161192368delinsACTGGCAGGGG	GRCh37
NC_000001.9:g.159458982_159458992delinsACTGGCAGGGG	NCBI36
NG_012043.1:g.6051_6061delinsCCCCTGCCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.186-56_186-46delinsCCCCTGCCAGT MANE Select	ENSP00000356969.3:n.186-56_186-46delinsCCCCTGCCAGT
ENST00000463273.5:c.186-56_186-46delinsCCCCTGCCAGT	ENSP00000476740.1:n.186-56_186-46delinsCCCCTGCCAGT
ENST00000463812.1:c.42-56_42-46delinsCCCCTGCCAGT	ENSP00000476890.1:n.42-56_42-46delinsCCCCTGCCAGT
ENST00000464492.5:c.285-56_285-46delinsCCCCTGCCAGT	ENSP00000476911.1:n.285-56_285-46delinsCCCCTGCCAGT
ENST00000468465.5:c.42-56_42-46delinsCCCCTGCCAGT	ENSP00000476662.1:n.42-56_42-46delinsCCCCTGCCAGT
ENST00000469730.2:c.186-56_186-46delinsCCCCTGCCAGT	ENSP00000476605.1:n.186-56_186-46delinsCCCCTGCCAGT
ENST00000470459.6:c.186-56_186-46delinsCCCCTGCCAGT	ENSP00000477031.1:n.186-56_186-46delinsCCCCTGCCAGT
ENST00000481413.1:n.697-56_697-46delinsCCCCTGCCAGT
ENST00000481511.5:c.*183-56_*183-46delinsCCCCTGCCAGT	ENSP00000477054.1:n.*183-56_*183-46delinsCCCCTGCCAGT
ENST00000491350.1:c.53-56_53-46delinsCCCCTGCCAGT	ENSP00000477353.1:n.53-56_53-46delinsCCCCTGCCAGT
NM_001643.1:c.186-56_186-46delinsCCCCTGCCAGT	NP_001634.1:n.186-56_186-46delinsCCCCTGCCAGT
NM_001643.2:c.186-56_186-46delinsCCCCTGCCAGT MANE Select	NP_001634.1:n.186-56_186-46delinsCCCCTGCCAGT