Canonical Allele Identifier: CA504895646

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1457068C>G , CM000681.2:g.1457068C>G	GRCh38
NC_000019.9:g.1457067C>G , CM000681.1:g.1457067C>G	GRCh37
NC_000019.8:g.1408067C>G	NCBI36
NG_055243.1:g.15801C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.1032C>G MANE Select	NP_005874.1:p.Arg344=
ENST00000590469.6:c.1032C>G MANE Select	ENSP00000467073.2:p.Arg344=
NM_001351273.1:c.1029C>G	NP_001338202.1:p.Arg343=
NM_005883.2:c.1032C>G	NP_005874.1:p.Arg344=
ENST00000233607.6:c.1032C>G	ENSP00000233607.2:p.Arg344=
ENST00000238483.5:c.1029C>G	ENSP00000238483.5:p.Arg343=
ENST00000535453.5:c.1032C>G	ENSP00000442954.1:p.Arg344=
ENST00000590469.5:c.1032C>G	ENSP00000467073.1:p.Arg344=
ENST00000593146.1:n.1091C>G
XM_005259475.2:c.1104C>G	XP_005259532.1:p.Arg368=
XM_006722607.2:c.1101C>G	XP_006722670.1:p.Arg367=
XM_006722608.2:c.1032C>G	XP_006722671.1:p.Arg344=
XM_006722608.3:c.1335C>G	XP_006722671.2:p.Arg445=
XM_006722609.2:c.1032C>G	XP_006722672.1:p.Arg344=
XM_006722609.3:c.1032C>G	XP_006722672.1:p.Arg344=
XM_006722610.2:c.1029C>G	XP_006722673.1:p.Arg343=
XM_006722610.3:c.1332C>G	XP_006722673.2:p.Arg444=