Canonical Allele Identifier: CA9045788

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1467446_1467451dup , CM000681.2:g.1467446_1467451dup	GRCh38
NC_000019.9:g.1467445_1467450dup , CM000681.1:g.1467445_1467450dup	GRCh37
NC_000019.8:g.1418445_1418450dup	NCBI36
NG_055243.1:g.26179_26184dup

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.4145_4150dup (APC2) MANE Select	NP_005874.1:p.Ala1383_Gln1384insProAla
ENST00000590469.6:c.4145_4150dup (APC2) MANE Select	ENSP00000467073.2:p.Ala1383_Gln1384insProAla
NM_001351273.1:c.4142_4147dup (APC2)	NP_001338202.1:p.Ala1382_Gln1383insProAla
NM_005883.2:c.4145_4150dup (APC2)	NP_005874.1:p.Ala1383_Gln1384insProAla
ENST00000233607.6:c.4145_4150dup (APC2)	ENSP00000233607.2:p.Ala1383_Gln1384insProAla
ENST00000535453.5:c.4145_4150dup (APC2)	ENSP00000442954.1:p.Ala1383_Gln1384insProAla
ENST00000588427.5:c.131-5617_131-5612dup (C19orf25)	ENSP00000468000.1:n.131-5617_131-5612dup
XM_005259475.2:c.4217_4222dup (APC2)	XP_005259532.1:p.Ala1407_Gln1408insProAla
XM_006722607.2:c.4214_4219dup (APC2)	XP_006722670.1:p.Ala1406_Gln1407insProAla
XM_006722608.2:c.4145_4150dup (APC2)	XP_006722671.1:p.Ala1383_Gln1384insProAla
XM_006722608.3:c.4448_4453dup (APC2)	XP_006722671.2:p.Ala1484_Gln1485insProAla
XM_006722609.2:c.4145_4150dup (APC2)	XP_006722672.1:p.Ala1383_Gln1384insProAla
XM_006722609.3:c.4145_4150dup (APC2)	XP_006722672.1:p.Ala1383_Gln1384insProAla
XM_006722610.2:c.4142_4147dup (APC2)	XP_006722673.1:p.Ala1382_Gln1383insProAla
XM_006722610.3:c.4445_4450dup (APC2)	XP_006722673.2:p.Ala1483_Gln1484insProAla