Canonical Allele Identifier: CA658760597

Gene: APC

Linked Data

• PubMed: PMID:10083733

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835070_112835072delinsCT , CM000667.2:g.112835070_112835072delinsCT	GRCh38
NC_000005.9:g.112170767_112170769delinsCT , CM000667.1:g.112170767_112170769delinsCT	GRCh37
NC_000005.8:g.112198666_112198668delinsCT	NCBI36
NG_008481.4:g.147550_147552delinsCT , LRG_130:g.147550_147552delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1528_1530delinsCT	ENSP00000484935.2:n.1528_1530delinsCT
ENST00000504915.3:c.1917_1919delinsCT	ENSP00000473355.2:p.Tyr640SerfsTer8
ENST00000505350.2:c.*1869_*1871delinsCT	ENSP00000481752.1:n.*1869_*1871delinsCT
ENST00000507379.6:c.1809_1811delinsCT	ENSP00000423224.2:p.Tyr604SerfsTer8
ENST00000509732.6:c.1863_1865delinsCT	ENSP00000426541.2:p.Tyr622SerfsTer8
ENST00000512211.7:c.1863_1865delinsCT	ENSP00000423828.3:p.Tyr622SerfsTer8
ENST00000257430.9:c.1863_1865delinsCT MANE Select	ENSP00000257430.4:p.Tyr622SerfsTer8
ENST00000257430.8:c.1863_1865delinsCT	ENSP00000257430.4:p.Tyr622SerfsTer8
ENST00000502371.2:c.216_218delinsCT
ENST00000504915.2:c.552_554delinsCT	ENSP00000473355.1:p.Tyr185SerfsTer8
ENST00000507379.5:c.1809_1811delinsCT	ENSP00000423224.1:p.Tyr604SerfsTer8
ENST00000508376.6:c.1863_1865delinsCT	ENSP00000427089.2:p.Tyr622SerfsTer8
ENST00000508624.5:c.*1185_*1187delinsCT	ENSP00000424265.1:n.*1185_*1187delinsCT
ENST00000512211.6:c.1863_1865delinsCT	ENSP00000423828.2:p.Tyr622SerfsTer8
ENST00000520401.1:c.230+6098_230+6100delinsCT
NM_000038.5:c.1863_1865delinsCT	NP_000029.2:p.Tyr622SerfsTer8
NM_001127510.2:c.1863_1865delinsCT	NP_001120982.1:p.Tyr622SerfsTer8
NM_001127511.2:c.1809_1811delinsCT	NP_001120983.2:p.Tyr604SerfsTer8
NM_001354895.1:c.1863_1865delinsCT	NP_001341824.1:p.Tyr622SerfsTer8
NM_001354896.1:c.1917_1919delinsCT	NP_001341825.1:p.Tyr640SerfsTer8
NM_001354897.1:c.1893_1895delinsCT	NP_001341826.1:p.Tyr632SerfsTer8
NM_001354898.1:c.1788_1790delinsCT	NP_001341827.1:p.Tyr597SerfsTer8
NM_001354899.1:c.1779_1781delinsCT	NP_001341828.1:p.Tyr594SerfsTer8
NM_001354900.1:c.1740_1742delinsCT	NP_001341829.1:p.Tyr581SerfsTer8
NM_001354901.1:c.1686_1688delinsCT	NP_001341830.1:p.Tyr563SerfsTer8
NM_001354902.1:c.1590_1592delinsCT	NP_001341831.1:p.Tyr531SerfsTer8
NM_001354903.1:c.1560_1562delinsCT	NP_001341832.1:p.Tyr521SerfsTer8
NM_001354904.1:c.1485_1487delinsCT	NP_001341833.1:p.Tyr496SerfsTer8
NM_001354905.1:c.1383_1385delinsCT	NP_001341834.1:p.Tyr462SerfsTer8
NM_001354906.1:c.1014_1016delinsCT	NP_001341835.1:p.Tyr339SerfsTer8
NM_000038.6:c.1863_1865delinsCT MANE Select	NP_000029.2:p.Tyr622SerfsTer8
NM_001127510.3:c.1863_1865delinsCT	NP_001120982.1:p.Tyr622SerfsTer8
NM_001127511.3:c.1809_1811delinsCT	NP_001120983.2:p.Tyr604SerfsTer8
NM_001354895.2:c.1863_1865delinsCT	NP_001341824.1:p.Tyr622SerfsTer8
NM_001354896.2:c.1917_1919delinsCT	NP_001341825.1:p.Tyr640SerfsTer8
NM_001354897.2:c.1893_1895delinsCT	NP_001341826.1:p.Tyr632SerfsTer8
NM_001354898.2:c.1788_1790delinsCT	NP_001341827.1:p.Tyr597SerfsTer8
NM_001354899.2:c.1779_1781delinsCT	NP_001341828.1:p.Tyr594SerfsTer8
NM_001354900.2:c.1740_1742delinsCT	NP_001341829.1:p.Tyr581SerfsTer8
NM_001354901.2:c.1686_1688delinsCT	NP_001341830.1:p.Tyr563SerfsTer8
NM_001354902.2:c.1590_1592delinsCT	NP_001341831.1:p.Tyr531SerfsTer8
NM_001354903.2:c.1560_1562delinsCT	NP_001341832.1:p.Tyr521SerfsTer8
NM_001354904.2:c.1485_1487delinsCT	NP_001341833.1:p.Tyr496SerfsTer8
NM_001354905.2:c.1383_1385delinsCT	NP_001341834.1:p.Tyr462SerfsTer8
NM_001354906.2:c.1014_1016delinsCT	NP_001341835.1:p.Tyr339SerfsTer8