Canonical Allele Identifier: CA9045796

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1467561G>C , CM000681.2:g.1467561G>C	GRCh38
NC_000019.9:g.1467560G>C , CM000681.1:g.1467560G>C	GRCh37
NC_000019.8:g.1418560G>C	NCBI36
NG_055243.1:g.26294G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.4260G>C (APC2) MANE Select	NP_005874.1:p.Gly1420=
ENST00000590469.6:c.4260G>C (APC2) MANE Select	ENSP00000467073.2:p.Gly1420=
NM_001351273.1:c.4257G>C (APC2)	NP_001338202.1:p.Gly1419=
NM_005883.2:c.4260G>C (APC2)	NP_005874.1:p.Gly1420=
ENST00000233607.6:c.4260G>C (APC2)	ENSP00000233607.2:p.Gly1420=
ENST00000535453.5:c.4260G>C (APC2)	ENSP00000442954.1:p.Gly1420=
ENST00000588427.5:c.131-5737C>G (C19orf25)	ENSP00000468000.1:n.131-5737C>G
XM_005259475.2:c.4332G>C (APC2)	XP_005259532.1:p.Gly1444=
XM_006722607.2:c.4329G>C (APC2)	XP_006722670.1:p.Gly1443=
XM_006722608.2:c.4260G>C (APC2)	XP_006722671.1:p.Gly1420=
XM_006722608.3:c.4563G>C (APC2)	XP_006722671.2:p.Gly1521=
XM_006722609.2:c.4260G>C (APC2)	XP_006722672.1:p.Gly1420=
XM_006722609.3:c.4260G>C (APC2)	XP_006722672.1:p.Gly1420=
XM_006722610.2:c.4257G>C (APC2)	XP_006722673.1:p.Gly1419=
XM_006722610.3:c.4560G>C (APC2)	XP_006722673.2:p.Gly1520=