Canonical Allele Identifier: CA1573505269

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827160_112827164delinsGCTTA , CM000667.2:g.112827160_112827164delinsGCTTA	GRCh38
NC_000005.9:g.112162857_112162861delinsGCTTA , CM000667.1:g.112162857_112162861delinsGCTTA	GRCh37
NC_000005.8:g.112190756_112190760delinsGCTTA	NCBI36
NG_008481.4:g.139640_139644delinsGCTTA , LRG_130:g.139640_139644delinsGCTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5169_1408+5173delinsGCTTA	ENSP00000484935.2:n.1408+5169_1408+5173de...
ENST00000504915.3:c.1515_1519delinsGCTTA	ENSP00000473355.2:p.Gly505=
ENST00000505084.2:n.1517_1521delinsGCTTA
ENST00000505350.2:c.*1467_*1471delinsGCTTA	ENSP00000481752.1:n.*1467_*1471delinsGCTT...
ENST00000507379.6:c.1407_1411delinsGCTTA	ENSP00000423224.2:p.Gly469=
ENST00000509732.6:c.1461_1465delinsGCTTA	ENSP00000426541.2:p.Gly487=
ENST00000512211.7:c.1461_1465delinsGCTTA	ENSP00000423828.3:p.Gly487=
ENST00000257430.9:c.1461_1465delinsGCTTA MANE Select	ENSP00000257430.4:p.Gly487=
ENST00000257430.8:c.1461_1465delinsGCTTA	ENSP00000257430.4:p.Gly487=
ENST00000502371.2:c.96+5169_96+5173delinsGCTTA
ENST00000504915.2:c.150_154delinsGCTTA	ENSP00000473355.1:p.Gly50=
ENST00000507379.5:c.1407_1411delinsGCTTA	ENSP00000423224.1:p.Gly469=
ENST00000508376.6:c.1461_1465delinsGCTTA	ENSP00000427089.2:p.Gly487=
ENST00000508624.5:c.*783_*787delinsGCTTA	ENSP00000424265.1:n.*783_*787delinsGCTTA
ENST00000512211.6:c.1461_1465delinsGCTTA	ENSP00000423828.2:p.Gly487=
NM_000038.5:c.1461_1465delinsGCTTA	NP_000029.2:p.Gly487=
NM_001127510.2:c.1461_1465delinsGCTTA	NP_001120982.1:p.Gly487=
NM_001127511.2:c.1407_1411delinsGCTTA	NP_001120983.2:p.Gly469=
NM_001354895.1:c.1461_1465delinsGCTTA	NP_001341824.1:p.Gly487=
NM_001354896.1:c.1515_1519delinsGCTTA	NP_001341825.1:p.Gly505=
NM_001354897.1:c.1491_1495delinsGCTTA	NP_001341826.1:p.Gly497=
NM_001354898.1:c.1386_1390delinsGCTTA	NP_001341827.1:p.Gly462=
NM_001354899.1:c.1377_1381delinsGCTTA	NP_001341828.1:p.Gly459=
NM_001354900.1:c.1338_1342delinsGCTTA	NP_001341829.1:p.Gly446=
NM_001354901.1:c.1284_1288delinsGCTTA	NP_001341830.1:p.Gly428=
NM_001354902.1:c.1188_1192delinsGCTTA	NP_001341831.1:p.Gly396=
NM_001354903.1:c.1158_1162delinsGCTTA	NP_001341832.1:p.Gly386=
NM_001354904.1:c.1083_1087delinsGCTTA	NP_001341833.1:p.Gly361=
NM_001354905.1:c.981_985delinsGCTTA	NP_001341834.1:p.Gly327=
NM_001354906.1:c.612_616delinsGCTTA	NP_001341835.1:p.Gly204=
NM_000038.6:c.1461_1465delinsGCTTA MANE Select	NP_000029.2:p.Gly487=
NM_001127510.3:c.1461_1465delinsGCTTA	NP_001120982.1:p.Gly487=
NM_001127511.3:c.1407_1411delinsGCTTA	NP_001120983.2:p.Gly469=
NM_001354895.2:c.1461_1465delinsGCTTA	NP_001341824.1:p.Gly487=
NM_001354896.2:c.1515_1519delinsGCTTA	NP_001341825.1:p.Gly505=
NM_001354897.2:c.1491_1495delinsGCTTA	NP_001341826.1:p.Gly497=
NM_001354898.2:c.1386_1390delinsGCTTA	NP_001341827.1:p.Gly462=
NM_001354899.2:c.1377_1381delinsGCTTA	NP_001341828.1:p.Gly459=
NM_001354900.2:c.1338_1342delinsGCTTA	NP_001341829.1:p.Gly446=
NM_001354901.2:c.1284_1288delinsGCTTA	NP_001341830.1:p.Gly428=
NM_001354902.2:c.1188_1192delinsGCTTA	NP_001341831.1:p.Gly396=
NM_001354903.2:c.1158_1162delinsGCTTA	NP_001341832.1:p.Gly386=
NM_001354904.2:c.1083_1087delinsGCTTA	NP_001341833.1:p.Gly361=
NM_001354905.2:c.981_985delinsGCTTA	NP_001341834.1:p.Gly327=
NM_001354906.2:c.612_616delinsGCTTA	NP_001341835.1:p.Gly204=