Canonical Allele Identifier: CA9044922

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1456918G>C , CM000681.2:g.1456918G>C	GRCh38
NC_000019.9:g.1456917G>C , CM000681.1:g.1456917G>C	GRCh37
NC_000019.8:g.1407917G>C	NCBI36
NG_055243.1:g.15651G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590469.6:c.882G>C MANE Select	ENSP00000467073.2:p.Thr294=
ENST00000233607.6:c.882G>C	ENSP00000233607.2:p.Thr294=
ENST00000238483.5:c.879G>C	ENSP00000238483.5:p.Thr293=
ENST00000535453.5:c.882G>C	ENSP00000442954.1:p.Thr294=
ENST00000590469.5:c.882G>C	ENSP00000467073.1:p.Thr294=
ENST00000593146.1:n.941G>C
NM_005883.2:c.882G>C	NP_005874.1:p.Thr294=
XM_005259475.2:c.954G>C	XP_005259532.1:p.Thr318=
XM_006722607.2:c.951G>C	XP_006722670.1:p.Thr317=
XM_006722608.2:c.882G>C	XP_006722671.1:p.Thr294=
XM_006722609.2:c.882G>C	XP_006722672.1:p.Thr294=
XM_006722610.2:c.879G>C	XP_006722673.1:p.Thr293=
NM_001351273.1:c.879G>C	NP_001338202.1:p.Thr293=
XM_006722608.3:c.1185G>C	XP_006722671.2:p.Thr395=
XM_006722609.3:c.882G>C	XP_006722672.1:p.Thr294=
XM_006722610.3:c.1182G>C	XP_006722673.2:p.Thr394=
NM_005883.3:c.882G>C MANE Select	NP_005874.1:p.Thr294=