Canonical Allele Identifier: CA1202652422

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222655_161222657delinsGCC , CM000663.2:g.161222655_161222657delinsGCC	GRCh38
NC_000001.10:g.161192445_161192447delinsGCC , CM000663.1:g.161192445_161192447delinsGCC	GRCh37
NC_000001.9:g.159459069_159459071delinsGCC	NCBI36
NG_012043.1:g.5972_5974delinsGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.186-135_186-133delinsGGC MANE Select	ENSP00000356969.3:n.186-135_186-133delinsGGC
ENST00000463273.5:c.186-135_186-133delinsGGC	ENSP00000476740.1:n.186-135_186-133delinsGGC
ENST00000463812.1:c.42-135_42-133delinsGGC	ENSP00000476890.1:n.42-135_42-133delinsGGC
ENST00000464492.5:c.285-135_285-133delinsGGC	ENSP00000476911.1:n.285-135_285-133delinsGGC
ENST00000468465.5:c.42-135_42-133delinsGGC	ENSP00000476662.1:n.42-135_42-133delinsGGC
ENST00000469730.2:c.186-135_186-133delinsGGC	ENSP00000476605.1:n.186-135_186-133delinsGGC
ENST00000470459.6:c.186-135_186-133delinsGGC	ENSP00000477031.1:n.186-135_186-133delinsGGC
ENST00000481413.1:n.697-135_697-133delinsGGC
ENST00000481511.5:c.*183-135_*183-133delinsGGC	ENSP00000477054.1:n.*183-135_*183-133delinsGGC
ENST00000491350.1:c.53-135_53-133delinsGGC	ENSP00000477353.1:n.53-135_53-133delinsGGC
NM_001643.1:c.186-135_186-133delinsGGC	NP_001634.1:n.186-135_186-133delinsGGC
NM_001643.2:c.186-135_186-133delinsGGC MANE Select	NP_001634.1:n.186-135_186-133delinsGGC