Canonical Allele Identifier: CA1573470772

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835035G= , CM000667.2:g.112835035G=	GRCh38
NC_000005.9:g.112170732G= , CM000667.1:g.112170732G=	GRCh37
NC_000005.8:g.112198631G=	NCBI36
NG_008481.4:g.147515G= , LRG_130:g.147515G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1493G=	ENSP00000484935.2:n.1493G=
ENST00000504915.3:c.1882G=	ENSP00000473355.2:p.Asp628=
ENST00000505350.2:c.*1834G=	ENSP00000481752.1:n.*1834G=
ENST00000507379.6:c.1774G=	ENSP00000423224.2:p.Asp592=
ENST00000509732.6:c.1828G=	ENSP00000426541.2:p.Asp610=
ENST00000512211.7:c.1828G=	ENSP00000423828.3:p.Asp610=
ENST00000257430.9:c.1828G= MANE Select	ENSP00000257430.4:p.Asp610=
ENST00000257430.8:c.1828G=	ENSP00000257430.4:p.Asp610=
ENST00000502371.2:c.181G=
ENST00000504915.2:c.517G=	ENSP00000473355.1:p.Asp173=
ENST00000507379.5:c.1774G=	ENSP00000423224.1:p.Asp592=
ENST00000508376.6:c.1828G=	ENSP00000427089.2:p.Asp610=
ENST00000508624.5:c.*1150G=	ENSP00000424265.1:n.*1150G=
ENST00000512211.6:c.1828G=	ENSP00000423828.2:p.Asp610=
ENST00000520401.1:c.230+6063G=
NM_000038.5:c.1828G=	NP_000029.2:p.Asp610=
NM_001127510.2:c.1828G=	NP_001120982.1:p.Asp610=
NM_001127511.2:c.1774G=	NP_001120983.2:p.Asp592=
NM_001354895.1:c.1828G=	NP_001341824.1:p.Asp610=
NM_001354896.1:c.1882G=	NP_001341825.1:p.Asp628=
NM_001354897.1:c.1858G=	NP_001341826.1:p.Asp620=
NM_001354898.1:c.1753G=	NP_001341827.1:p.Asp585=
NM_001354899.1:c.1744G=	NP_001341828.1:p.Asp582=
NM_001354900.1:c.1705G=	NP_001341829.1:p.Asp569=
NM_001354901.1:c.1651G=	NP_001341830.1:p.Asp551=
NM_001354902.1:c.1555G=	NP_001341831.1:p.Asp519=
NM_001354903.1:c.1525G=	NP_001341832.1:p.Asp509=
NM_001354904.1:c.1450G=	NP_001341833.1:p.Asp484=
NM_001354905.1:c.1348G=	NP_001341834.1:p.Asp450=
NM_001354906.1:c.979G=	NP_001341835.1:p.Asp327=
NM_000038.6:c.1828G= MANE Select	NP_000029.2:p.Asp610=
NM_001127510.3:c.1828G=	NP_001120982.1:p.Asp610=
NM_001127511.3:c.1774G=	NP_001120983.2:p.Asp592=
NM_001354895.2:c.1828G=	NP_001341824.1:p.Asp610=
NM_001354896.2:c.1882G=	NP_001341825.1:p.Asp628=
NM_001354897.2:c.1858G=	NP_001341826.1:p.Asp620=
NM_001354898.2:c.1753G=	NP_001341827.1:p.Asp585=
NM_001354899.2:c.1744G=	NP_001341828.1:p.Asp582=
NM_001354900.2:c.1705G=	NP_001341829.1:p.Asp569=
NM_001354901.2:c.1651G=	NP_001341830.1:p.Asp551=
NM_001354902.2:c.1555G=	NP_001341831.1:p.Asp519=
NM_001354903.2:c.1525G=	NP_001341832.1:p.Asp509=
NM_001354904.2:c.1450G=	NP_001341833.1:p.Asp484=
NM_001354905.2:c.1348G=	NP_001341834.1:p.Asp450=
NM_001354906.2:c.979G=	NP_001341835.1:p.Asp327=