Canonical Allele Identifier: CA9045938

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1468258C>G , CM000681.2:g.1468258C>G	GRCh38
NC_000019.9:g.1468257C>G , CM000681.1:g.1468257C>G	GRCh37
NC_000019.8:g.1419257C>G	NCBI36
NG_055243.1:g.26991C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590469.6:c.4957C>G (APC2) MANE Select	ENSP00000467073.2:p.Arg1653Gly
ENST00000233607.6:c.4957C>G (APC2)	ENSP00000233607.2:p.Arg1653Gly
ENST00000535453.5:c.4957C>G (APC2)	ENSP00000442954.1:p.Arg1653Gly
ENST00000588427.5:c.131-6434G>C (C19orf25)	ENSP00000468000.1:n.131-6434G>C
NM_005883.2:c.4957C>G (APC2)	NP_005874.1:p.Arg1653Gly
XM_005259475.2:c.5029C>G (APC2)	XP_005259532.1:p.Arg1677Gly
XM_006722607.2:c.5026C>G (APC2)	XP_006722670.1:p.Arg1676Gly
XM_006722608.2:c.4957C>G (APC2)	XP_006722671.1:p.Arg1653Gly
XM_006722609.2:c.4957C>G (APC2)	XP_006722672.1:p.Arg1653Gly
XM_006722610.2:c.4954C>G (APC2)	XP_006722673.1:p.Arg1652Gly
NM_001351273.1:c.4954C>G (APC2)	NP_001338202.1:p.Arg1652Gly
XM_006722608.3:c.5260C>G (APC2)	XP_006722671.2:p.Arg1754Gly
XM_006722609.3:c.4957C>G (APC2)	XP_006722672.1:p.Arg1653Gly
XM_006722610.3:c.5257C>G (APC2)	XP_006722673.2:p.Arg1753Gly
NM_005883.3:c.4957C>G (APC2) MANE Select	NP_005874.1:p.Arg1653Gly