Canonical Allele Identifier: CA9044807

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1455518dup , CM000681.2:g.1455518dup	GRCh38
NC_000019.9:g.1455517dup , CM000681.1:g.1455517dup	GRCh37
NC_000019.8:g.1406517dup	NCBI36
NG_055243.1:g.14251dup

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.639+18dup MANE Select	NP_005874.1:n.639+18dup
ENST00000590469.6:c.639+18dup MANE Select	ENSP00000467073.2:n.639+18dup
NM_001351273.1:c.636+18dup	NP_001338202.1:n.636+18dup
NM_005883.2:c.639+18dup	NP_005874.1:n.639+18dup
ENST00000233607.6:c.639+18dup	ENSP00000233607.2:n.639+18dup
ENST00000238483.5:c.636+18dup	ENSP00000238483.5:n.636+18dup
ENST00000535453.5:c.639+18dup	ENSP00000442954.1:n.639+18dup
ENST00000590469.5:c.639+18dup	ENSP00000467073.1:n.639+18dup
ENST00000593146.1:n.698+18dup
XM_005259475.2:c.711+18dup	XP_005259532.1:n.711+18dup
XM_006722607.2:c.708+18dup	XP_006722670.1:n.708+18dup
XM_006722608.2:c.639+18dup	XP_006722671.1:n.639+18dup
XM_006722608.3:c.942+18dup	XP_006722671.2:n.942+18dup
XM_006722609.2:c.639+18dup	XP_006722672.1:n.639+18dup
XM_006722609.3:c.639+18dup	XP_006722672.1:n.639+18dup
XM_006722610.2:c.636+18dup	XP_006722673.1:n.636+18dup
XM_006722610.3:c.939+18dup	XP_006722673.2:n.939+18dup