Canonical Allele Identifier: CA446206660

Gene: APC

Linked Data

• COSMIC: COSM18866
• MyVariant Identifiers: chr5:g.112175960_112175961insA (hg19) ; chr5:g.112175959_112175960insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840263dup , CM000667.2:g.112840263dup	GRCh38
NC_000005.9:g.112175960dup , CM000667.1:g.112175960dup	GRCh37
NC_000005.8:g.112203859dup	NCBI36
NG_008481.4:g.152743dup , LRG_130:g.152743dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4723dup	ENSP00000473355.2:p.Ile1575AsnfsTer2
ENST00000505350.2:c.*4675dup	ENSP00000481752.1:n.*4675dup
ENST00000507379.6:c.4615dup	ENSP00000423224.2:p.Ile1539AsnfsTer2
ENST00000509732.6:c.4669dup	ENSP00000426541.2:p.Ile1557AsnfsTer2
ENST00000512211.7:c.4669dup	ENSP00000423828.3:p.Ile1557AsnfsTer2
ENST00000257430.9:c.4669dup MANE Select	ENSP00000257430.4:p.Ile1557AsnfsTer2
ENST00000257430.8:c.4669dup	ENSP00000257430.4:p.Ile1557AsnfsTer2
ENST00000508376.6:c.4669dup	ENSP00000427089.2:p.Ile1557AsnfsTer2
ENST00000508624.5:c.*3991dup	ENSP00000424265.1:n.*3991dup
ENST00000520401.1:c.230+11291dup
NM_000038.5:c.4669dup	NP_000029.2:p.Ile1557AsnfsTer2
NM_001127510.2:c.4669dup	NP_001120982.1:p.Ile1557AsnfsTer2
NM_001127511.2:c.4615dup	NP_001120983.2:p.Ile1539AsnfsTer2
NM_001354895.1:c.4669dup	NP_001341824.1:p.Ile1557AsnfsTer2
NM_001354896.1:c.4723dup	NP_001341825.1:p.Ile1575AsnfsTer2
NM_001354897.1:c.4699dup	NP_001341826.1:p.Ile1567AsnfsTer2
NM_001354898.1:c.4594dup	NP_001341827.1:p.Ile1532AsnfsTer2
NM_001354899.1:c.4585dup	NP_001341828.1:p.Ile1529AsnfsTer2
NM_001354900.1:c.4546dup	NP_001341829.1:p.Ile1516AsnfsTer2
NM_001354901.1:c.4492dup	NP_001341830.1:p.Ile1498AsnfsTer2
NM_001354902.1:c.4396dup	NP_001341831.1:p.Ile1466AsnfsTer2
NM_001354903.1:c.4366dup	NP_001341832.1:p.Ile1456AsnfsTer2
NM_001354904.1:c.4291dup	NP_001341833.1:p.Ile1431AsnfsTer2
NM_001354905.1:c.4189dup	NP_001341834.1:p.Ile1397AsnfsTer2
NM_001354906.1:c.3820dup	NP_001341835.1:p.Ile1274AsnfsTer2
NM_000038.6:c.4669dup MANE Select	NP_000029.2:p.Ile1557AsnfsTer2
NM_001127510.3:c.4669dup	NP_001120982.1:p.Ile1557AsnfsTer2
NM_001127511.3:c.4615dup	NP_001120983.2:p.Ile1539AsnfsTer2
NM_001354895.2:c.4669dup	NP_001341824.1:p.Ile1557AsnfsTer2
NM_001354896.2:c.4723dup	NP_001341825.1:p.Ile1575AsnfsTer2
NM_001354897.2:c.4699dup	NP_001341826.1:p.Ile1567AsnfsTer2
NM_001354898.2:c.4594dup	NP_001341827.1:p.Ile1532AsnfsTer2
NM_001354899.2:c.4585dup	NP_001341828.1:p.Ile1529AsnfsTer2
NM_001354900.2:c.4546dup	NP_001341829.1:p.Ile1516AsnfsTer2
NM_001354901.2:c.4492dup	NP_001341830.1:p.Ile1498AsnfsTer2
NM_001354902.2:c.4396dup	NP_001341831.1:p.Ile1466AsnfsTer2
NM_001354903.2:c.4366dup	NP_001341832.1:p.Ile1456AsnfsTer2
NM_001354904.2:c.4291dup	NP_001341833.1:p.Ile1431AsnfsTer2
NM_001354905.2:c.4189dup	NP_001341834.1:p.Ile1397AsnfsTer2
NM_001354906.2:c.3820dup	NP_001341835.1:p.Ile1274AsnfsTer2