Canonical Allele Identifier: CA1573472323

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840493_112840494delinsAC , CM000667.2:g.112840493_112840494delinsAC	GRCh38
NC_000005.9:g.112176190_112176191delinsAC , CM000667.1:g.112176190_112176191delinsAC	GRCh37
NC_000005.8:g.112204089_112204090delinsAC	NCBI36
NG_008481.4:g.152973_152974delinsAC , LRG_130:g.152973_152974delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4953_4954delinsAC	ENSP00000473355.2:p.Thr1651=
ENST00000505350.2:c.*4905_*4906delinsAC	ENSP00000481752.1:n.*4905_*4906delinsAC
ENST00000507379.6:c.4845_4846delinsAC	ENSP00000423224.2:p.Thr1615=
ENST00000509732.6:c.4899_4900delinsAC	ENSP00000426541.2:p.Thr1633=
ENST00000512211.7:c.4899_4900delinsAC	ENSP00000423828.3:p.Thr1633=
ENST00000257430.9:c.4899_4900delinsAC MANE Select	ENSP00000257430.4:p.Thr1633=
ENST00000257430.8:c.4899_4900delinsAC	ENSP00000257430.4:p.Thr1633=
ENST00000508376.6:c.4899_4900delinsAC	ENSP00000427089.2:p.Thr1633=
ENST00000508624.5:c.*4221_*4222delinsAC	ENSP00000424265.1:n.*4221_*4222delinsAC
ENST00000520401.1:c.230+11521_230+11522delinsAC
NM_000038.5:c.4899_4900delinsAC	NP_000029.2:p.Thr1633=
NM_001127510.2:c.4899_4900delinsAC	NP_001120982.1:p.Thr1633=
NM_001127511.2:c.4845_4846delinsAC	NP_001120983.2:p.Thr1615=
NM_001354895.1:c.4899_4900delinsAC	NP_001341824.1:p.Thr1633=
NM_001354896.1:c.4953_4954delinsAC	NP_001341825.1:p.Thr1651=
NM_001354897.1:c.4929_4930delinsAC	NP_001341826.1:p.Thr1643=
NM_001354898.1:c.4824_4825delinsAC	NP_001341827.1:p.Thr1608=
NM_001354899.1:c.4815_4816delinsAC	NP_001341828.1:p.Thr1605=
NM_001354900.1:c.4776_4777delinsAC	NP_001341829.1:p.Thr1592=
NM_001354901.1:c.4722_4723delinsAC	NP_001341830.1:p.Thr1574=
NM_001354902.1:c.4626_4627delinsAC	NP_001341831.1:p.Thr1542=
NM_001354903.1:c.4596_4597delinsAC	NP_001341832.1:p.Thr1532=
NM_001354904.1:c.4521_4522delinsAC	NP_001341833.1:p.Thr1507=
NM_001354905.1:c.4419_4420delinsAC	NP_001341834.1:p.Thr1473=
NM_001354906.1:c.4050_4051delinsAC	NP_001341835.1:p.Thr1350=
NM_000038.6:c.4899_4900delinsAC MANE Select	NP_000029.2:p.Thr1633=
NM_001127510.3:c.4899_4900delinsAC	NP_001120982.1:p.Thr1633=
NM_001127511.3:c.4845_4846delinsAC	NP_001120983.2:p.Thr1615=
NM_001354895.2:c.4899_4900delinsAC	NP_001341824.1:p.Thr1633=
NM_001354896.2:c.4953_4954delinsAC	NP_001341825.1:p.Thr1651=
NM_001354897.2:c.4929_4930delinsAC	NP_001341826.1:p.Thr1643=
NM_001354898.2:c.4824_4825delinsAC	NP_001341827.1:p.Thr1608=
NM_001354899.2:c.4815_4816delinsAC	NP_001341828.1:p.Thr1605=
NM_001354900.2:c.4776_4777delinsAC	NP_001341829.1:p.Thr1592=
NM_001354901.2:c.4722_4723delinsAC	NP_001341830.1:p.Thr1574=
NM_001354902.2:c.4626_4627delinsAC	NP_001341831.1:p.Thr1542=
NM_001354903.2:c.4596_4597delinsAC	NP_001341832.1:p.Thr1532=
NM_001354904.2:c.4521_4522delinsAC	NP_001341833.1:p.Thr1507=
NM_001354905.2:c.4419_4420delinsAC	NP_001341834.1:p.Thr1473=
NM_001354906.2:c.4050_4051delinsAC	NP_001341835.1:p.Thr1350=