Canonical Allele Identifier: CA1141650776

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222437C= , CM000663.2:g.161222437C=	GRCh38
NC_000001.10:g.161192227C= , CM000663.1:g.161192227C=	GRCh37
NC_000001.9:g.159458851C=	NCBI36
NG_012043.1:g.6192G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.271G= MANE Select	ENSP00000356969.3:p.Val91=
ENST00000463273.5:c.271G=	ENSP00000476740.1:p.Val91=
ENST00000463812.1:c.127G=	ENSP00000476890.1:p.Val43=
ENST00000464492.5:c.370G=	ENSP00000476911.1:p.Val124=
ENST00000468465.5:c.127G=	ENSP00000476662.1:p.Val43=
ENST00000470459.6:c.217G=	ENSP00000477031.1:p.Val73=
ENST00000481413.1:n.782G=
ENST00000481511.5:c.*268G=	ENSP00000477054.1:n.*268G=
ENST00000491350.1:c.*54G=	ENSP00000477353.1:n.*54G=
NM_001643.1:c.271G=	NP_001634.1:p.Val91=
NM_001643.2:c.271G= MANE Select	NP_001634.1:p.Val91=