Canonical Allele Identifier: CA2697546421

Gene: APC

Linked Data

• ClinVar Variation Id: 2755853
• ClinVar RCV Id: RCV003536849

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840491dup , CM000667.2:g.112840491dup	GRCh38
NC_000005.9:g.112176188dup , CM000667.1:g.112176188dup	GRCh37
NC_000005.8:g.112204087dup	NCBI36
NG_008481.4:g.152971dup , LRG_130:g.152971dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4951dup	ENSP00000473355.2:p.Thr1651AsnfsTer5
ENST00000505350.2:c.*4903dup	ENSP00000481752.1:n.*4903dup
ENST00000507379.6:c.4843dup	ENSP00000423224.2:p.Thr1615AsnfsTer5
ENST00000509732.6:c.4897dup	ENSP00000426541.2:p.Thr1633AsnfsTer5
ENST00000512211.7:c.4897dup	ENSP00000423828.3:p.Thr1633AsnfsTer5
ENST00000257430.9:c.4897dup MANE Select	ENSP00000257430.4:p.Thr1633AsnfsTer5
ENST00000257430.8:c.4897dup	ENSP00000257430.4:p.Thr1633AsnfsTer5
ENST00000508376.6:c.4897dup	ENSP00000427089.2:p.Thr1633AsnfsTer5
ENST00000508624.5:c.*4219dup	ENSP00000424265.1:n.*4219dup
ENST00000520401.1:c.230+11519dup
NM_000038.5:c.4897dup	NP_000029.2:p.Thr1633AsnfsTer5
NM_001127510.2:c.4897dup	NP_001120982.1:p.Thr1633AsnfsTer5
NM_001127511.2:c.4843dup	NP_001120983.2:p.Thr1615AsnfsTer5
NM_001354895.1:c.4897dup	NP_001341824.1:p.Thr1633AsnfsTer5
NM_001354896.1:c.4951dup	NP_001341825.1:p.Thr1651AsnfsTer5
NM_001354897.1:c.4927dup	NP_001341826.1:p.Thr1643AsnfsTer5
NM_001354898.1:c.4822dup	NP_001341827.1:p.Thr1608AsnfsTer5
NM_001354899.1:c.4813dup	NP_001341828.1:p.Thr1605AsnfsTer5
NM_001354900.1:c.4774dup	NP_001341829.1:p.Thr1592AsnfsTer5
NM_001354901.1:c.4720dup	NP_001341830.1:p.Thr1574AsnfsTer5
NM_001354902.1:c.4624dup	NP_001341831.1:p.Thr1542AsnfsTer5
NM_001354903.1:c.4594dup	NP_001341832.1:p.Thr1532AsnfsTer5
NM_001354904.1:c.4519dup	NP_001341833.1:p.Thr1507AsnfsTer5
NM_001354905.1:c.4417dup	NP_001341834.1:p.Thr1473AsnfsTer5
NM_001354906.1:c.4048dup	NP_001341835.1:p.Thr1350AsnfsTer5
NM_000038.6:c.4897dup MANE Select	NP_000029.2:p.Thr1633AsnfsTer5
NM_001127510.3:c.4897dup	NP_001120982.1:p.Thr1633AsnfsTer5
NM_001127511.3:c.4843dup	NP_001120983.2:p.Thr1615AsnfsTer5
NM_001354895.2:c.4897dup	NP_001341824.1:p.Thr1633AsnfsTer5
NM_001354896.2:c.4951dup	NP_001341825.1:p.Thr1651AsnfsTer5
NM_001354897.2:c.4927dup	NP_001341826.1:p.Thr1643AsnfsTer5
NM_001354898.2:c.4822dup	NP_001341827.1:p.Thr1608AsnfsTer5
NM_001354899.2:c.4813dup	NP_001341828.1:p.Thr1605AsnfsTer5
NM_001354900.2:c.4774dup	NP_001341829.1:p.Thr1592AsnfsTer5
NM_001354901.2:c.4720dup	NP_001341830.1:p.Thr1574AsnfsTer5
NM_001354902.2:c.4624dup	NP_001341831.1:p.Thr1542AsnfsTer5
NM_001354903.2:c.4594dup	NP_001341832.1:p.Thr1532AsnfsTer5
NM_001354904.2:c.4519dup	NP_001341833.1:p.Thr1507AsnfsTer5
NM_001354905.2:c.4417dup	NP_001341834.1:p.Thr1473AsnfsTer5
NM_001354906.2:c.4048dup	NP_001341835.1:p.Thr1350AsnfsTer5