Canonical Allele Identifier: CA9045552

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1466146G>A , CM000681.2:g.1466146G>A	GRCh38
NC_000019.9:g.1466145G>A , CM000681.1:g.1466145G>A	GRCh37
NC_000019.8:g.1417145G>A	NCBI36
NG_055243.1:g.24879G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.2845G>A (APC2) MANE Select	NP_005874.1:p.Ala949Thr
ENST00000590469.6:c.2845G>A (APC2) MANE Select	ENSP00000467073.2:p.Ala949Thr
NM_001351273.1:c.2842G>A (APC2)	NP_001338202.1:p.Ala948Thr
NM_005883.2:c.2845G>A (APC2)	NP_005874.1:p.Ala949Thr
ENST00000233607.6:c.2845G>A (APC2)	ENSP00000233607.2:p.Ala949Thr
ENST00000535453.5:c.2845G>A (APC2)	ENSP00000442954.1:p.Ala949Thr
ENST00000588427.5:c.131-4322C>T (C19orf25)	ENSP00000468000.1:n.131-4322C>T
XM_005259475.2:c.2917G>A (APC2)	XP_005259532.1:p.Ala973Thr
XM_006722607.2:c.2914G>A (APC2)	XP_006722670.1:p.Ala972Thr
XM_006722608.2:c.2845G>A (APC2)	XP_006722671.1:p.Ala949Thr
XM_006722608.3:c.3148G>A (APC2)	XP_006722671.2:p.Ala1050Thr
XM_006722609.2:c.2845G>A (APC2)	XP_006722672.1:p.Ala949Thr
XM_006722609.3:c.2845G>A (APC2)	XP_006722672.1:p.Ala949Thr
XM_006722610.2:c.2842G>A (APC2)	XP_006722673.1:p.Ala948Thr
XM_006722610.3:c.3145G>A (APC2)	XP_006722673.2:p.Ala1049Thr