Canonical Allele Identifier: CA1202652479

Gene: APOA2

Linked Data

• dbSNP Id: rs1666192151
• gnomAD v4: 1-161222781-A-AAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222783_161222785dup , CM000663.2:g.161222783_161222785dup	GRCh38
NC_000001.10:g.161192573_161192575dup , CM000663.1:g.161192573_161192575dup	GRCh37
NC_000001.9:g.159459197_159459199dup	NCBI36
NG_012043.1:g.5845_5847dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.185+134_185+136dup MANE Select	ENSP00000356969.3:n.185+134_185+136dup
ENST00000463273.5:c.185+134_185+136dup	ENSP00000476740.1:n.185+134_185+136dup
ENST00000463812.1:c.41+134_41+136dup	ENSP00000476890.1:n.41+134_41+136dup
ENST00000464492.5:c.284+134_284+136dup	ENSP00000476911.1:n.284+134_284+136dup
ENST00000468465.5:c.41+134_41+136dup	ENSP00000476662.1:n.41+134_41+136dup
ENST00000469730.2:c.185+134_185+136dup	ENSP00000476605.1:n.185+134_185+136dup
ENST00000470459.6:c.185+134_185+136dup	ENSP00000477031.1:n.185+134_185+136dup
ENST00000481413.1:n.696+134_696+136dup
ENST00000481511.5:c.*182+134_*182+136dup	ENSP00000477054.1:n.*182+134_*182+136dup
ENST00000491350.1:c.53-262_53-260dup	ENSP00000477353.1:n.53-262_53-260dup
NM_001643.1:c.185+134_185+136dup	NP_001634.1:n.185+134_185+136dup
NM_001643.2:c.185+134_185+136dup MANE Select	NP_001634.1:n.185+134_185+136dup