Canonical Allele Identifier: CA403038319

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1468114G>A , CM000681.2:g.1468114G>A	GRCh38
NC_000019.9:g.1468113G>A , CM000681.1:g.1468113G>A	GRCh37
NC_000019.8:g.1419113G>A	NCBI36
NG_055243.1:g.26847G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590469.6:c.4813G>A (APC2) MANE Select	ENSP00000467073.2:p.Ala1605Thr
ENST00000233607.6:c.4813G>A (APC2)	ENSP00000233607.2:p.Ala1605Thr
ENST00000535453.5:c.4813G>A (APC2)	ENSP00000442954.1:p.Ala1605Thr
ENST00000588427.5:c.131-6290C>T (C19orf25)	ENSP00000468000.1:n.131-6290C>T
NM_005883.2:c.4813G>A (APC2)	NP_005874.1:p.Ala1605Thr
XM_005259475.2:c.4885G>A (APC2)	XP_005259532.1:p.Ala1629Thr
XM_006722607.2:c.4882G>A (APC2)	XP_006722670.1:p.Ala1628Thr
XM_006722608.2:c.4813G>A (APC2)	XP_006722671.1:p.Ala1605Thr
XM_006722609.2:c.4813G>A (APC2)	XP_006722672.1:p.Ala1605Thr
XM_006722610.2:c.4810G>A (APC2)	XP_006722673.1:p.Ala1604Thr
NM_001351273.1:c.4810G>A (APC2)	NP_001338202.1:p.Ala1604Thr
XM_006722608.3:c.5116G>A (APC2)	XP_006722671.2:p.Ala1706Thr
XM_006722609.3:c.4813G>A (APC2)	XP_006722672.1:p.Ala1605Thr
XM_006722610.3:c.5113G>A (APC2)	XP_006722673.2:p.Ala1705Thr
NM_005883.3:c.4813G>A (APC2) MANE Select	NP_005874.1:p.Ala1605Thr