Canonical Allele Identifier: CA9044838

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1456123G>A , CM000681.2:g.1456123G>A	GRCh38
NC_000019.9:g.1456122G>A , CM000681.1:g.1456122G>A	GRCh37
NC_000019.8:g.1407122G>A	NCBI36
NG_055243.1:g.14856G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590469.6:c.687G>A MANE Select	ENSP00000467073.2:p.Ala229=
ENST00000233607.6:c.687G>A	ENSP00000233607.2:p.Ala229=
ENST00000238483.5:c.684G>A	ENSP00000238483.5:p.Ala228=
ENST00000535453.5:c.687G>A	ENSP00000442954.1:p.Ala229=
ENST00000590469.5:c.687G>A	ENSP00000467073.1:p.Ala229=
ENST00000593146.1:n.746G>A
NM_005883.2:c.687G>A	NP_005874.1:p.Ala229=
XM_005259475.2:c.759G>A	XP_005259532.1:p.Ala253=
XM_006722607.2:c.756G>A	XP_006722670.1:p.Ala252=
XM_006722608.2:c.687G>A	XP_006722671.1:p.Ala229=
XM_006722609.2:c.687G>A	XP_006722672.1:p.Ala229=
XM_006722610.2:c.684G>A	XP_006722673.1:p.Ala228=
NM_001351273.1:c.684G>A	NP_001338202.1:p.Ala228=
XM_006722608.3:c.990G>A	XP_006722671.2:p.Ala330=
XM_006722609.3:c.687G>A	XP_006722672.1:p.Ala229=
XM_006722610.3:c.987G>A	XP_006722673.2:p.Ala329=
NM_005883.3:c.687G>A MANE Select	NP_005874.1:p.Ala229=