Canonical Allele Identifier: CA403010707

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1453575C>G , CM000681.2:g.1453575C>G	GRCh38
NC_000019.9:g.1453574C>G , CM000681.1:g.1453574C>G	GRCh37
NC_000019.8:g.1404574C>G	NCBI36
NG_055243.1:g.12308C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587149.6:c.377C>G	ENSP00000468199.2:p.Ala126Gly
ENST00000590469.6:c.377C>G MANE Select	ENSP00000467073.2:p.Ala126Gly
ENST00000233607.6:c.377C>G	ENSP00000233607.2:p.Ala126Gly
ENST00000238483.5:c.377C>G	ENSP00000238483.5:p.Ala126Gly
ENST00000535453.5:c.377C>G	ENSP00000442954.1:p.Ala126Gly
ENST00000587149.5:c.377C>G	ENSP00000468199.1:p.Ala126Gly
ENST00000587869.5:c.377C>G	ENSP00000466803.2:p.Ala126Gly
ENST00000590469.5:c.377C>G	ENSP00000467073.1:p.Ala126Gly
ENST00000590877.5:c.377C>G	ENSP00000466173.2:p.Ala126Gly
ENST00000593146.1:n.439C>G
NM_005883.2:c.377C>G	NP_005874.1:p.Ala126Gly
XM_005259475.2:c.449C>G	XP_005259532.1:p.Ala150Gly
XM_006722607.2:c.449C>G	XP_006722670.1:p.Ala150Gly
XM_006722608.2:c.377C>G	XP_006722671.1:p.Ala126Gly
XM_006722609.2:c.377C>G	XP_006722672.1:p.Ala126Gly
XM_006722610.2:c.377C>G	XP_006722673.1:p.Ala126Gly
NM_001351273.1:c.377C>G	NP_001338202.1:p.Ala126Gly
XM_006722608.3:c.680C>G	XP_006722671.2:p.Ala227Gly
XM_006722609.3:c.377C>G	XP_006722672.1:p.Ala126Gly
XM_006722610.3:c.680C>G	XP_006722673.2:p.Ala227Gly
NM_005883.3:c.377C>G MANE Select	NP_005874.1:p.Ala126Gly