Canonical Allele Identifier: CA9044956

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1457122C>A , CM000681.2:g.1457122C>A	GRCh38
NC_000019.9:g.1457121C>A , CM000681.1:g.1457121C>A	GRCh37
NC_000019.8:g.1408121C>A	NCBI36
NG_055243.1:g.15855C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590469.6:c.1086C>A MANE Select	ENSP00000467073.2:p.Gly362=
ENST00000233607.6:c.1086C>A	ENSP00000233607.2:p.Gly362=
ENST00000238483.5:c.1083C>A	ENSP00000238483.5:p.Gly361=
ENST00000535453.5:c.1086C>A	ENSP00000442954.1:p.Gly362=
ENST00000590469.5:c.1086C>A	ENSP00000467073.1:p.Gly362=
ENST00000593146.1:n.1145C>A
NM_005883.2:c.1086C>A	NP_005874.1:p.Gly362=
XM_005259475.2:c.1158C>A	XP_005259532.1:p.Gly386=
XM_006722607.2:c.1155C>A	XP_006722670.1:p.Gly385=
XM_006722608.2:c.1086C>A	XP_006722671.1:p.Gly362=
XM_006722609.2:c.1086C>A	XP_006722672.1:p.Gly362=
XM_006722610.2:c.1083C>A	XP_006722673.1:p.Gly361=
NM_001351273.1:c.1083C>A	NP_001338202.1:p.Gly361=
XM_006722608.3:c.1389C>A	XP_006722671.2:p.Gly463=
XM_006722609.3:c.1086C>A	XP_006722672.1:p.Gly362=
XM_006722610.3:c.1386C>A	XP_006722673.2:p.Gly462=
NM_005883.3:c.1086C>A MANE Select	NP_005874.1:p.Gly362=