Canonical Allele Identifier: CA2838416132

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222511dup , CM000663.2:g.161222511dup	GRCh38
NC_000001.10:g.161192301dup , CM000663.1:g.161192301dup	GRCh37
NC_000001.9:g.159458925dup	NCBI36
NG_012043.1:g.6121dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.200dup MANE Select	ENSP00000356969.3:p.Ser68ValfsTer18
ENST00000463273.5:c.200dup	ENSP00000476740.1:p.Ser68ValfsTer18
ENST00000463812.1:c.56dup	ENSP00000476890.1:p.Ser20ValfsTer18
ENST00000464492.5:c.299dup	ENSP00000476911.1:p.Ser101ValfsTer18
ENST00000468465.5:c.56dup	ENSP00000476662.1:p.Ser20ValfsTer18
ENST00000470459.6:c.200dup	ENSP00000477031.1:p.Asn67LysfsTer31
ENST00000481413.1:n.711dup
ENST00000481511.5:c.*197dup	ENSP00000477054.1:n.*197dup
ENST00000491350.1:c.67dup	ENSP00000477353.1:p.Ser23LysfsTer?
NM_001643.1:c.200dup	NP_001634.1:p.Ser68ValfsTer18
NM_001643.2:c.200dup MANE Select	NP_001634.1:p.Ser68ValfsTer18