Canonical Allele Identifier: CA645562798

Gene: APC

Linked Data

• COSMIC: COSM4169180

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828865_112828868del , CM000667.2:g.112828865_112828868del	GRCh38
NC_000005.9:g.112164562_112164565del , CM000667.1:g.112164562_112164565del	GRCh37
NC_000005.8:g.112192461_112192464del	NCBI36
NG_008481.4:g.141345_141348del , LRG_130:g.141345_141348del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6086_1409-6083del	ENSP00000484935.2:n.1409-6086_1409-6083de...
ENST00000504915.3:c.1690_1693del	ENSP00000473355.2:p.Ser564PhefsTer2
ENST00000505084.2:n.1692_1695del
ENST00000505350.2:c.*1642_*1645del	ENSP00000481752.1:n.*1642_*1645del
ENST00000507379.6:c.1582_1585del	ENSP00000423224.2:p.Ser528PhefsTer2
ENST00000509732.6:c.1636_1639del	ENSP00000426541.2:p.Ser546PhefsTer2
ENST00000512211.7:c.1636_1639del	ENSP00000423828.3:p.Ser546PhefsTer2
ENST00000257430.9:c.1636_1639del MANE Select	ENSP00000257430.4:p.Ser546PhefsTer2
ENST00000257430.8:c.1636_1639del	ENSP00000257430.4:p.Ser546PhefsTer2
ENST00000502371.2:c.97-6086_97-6083del
ENST00000504915.2:c.325_328del	ENSP00000473355.1:p.Ser109PhefsTer2
ENST00000505084.1:n.123_126del
ENST00000507379.5:c.1582_1585del	ENSP00000423224.1:p.Ser528PhefsTer2
ENST00000508376.6:c.1636_1639del	ENSP00000427089.2:p.Ser546PhefsTer2
ENST00000508624.5:c.*958_*961del	ENSP00000424265.1:n.*958_*961del
ENST00000512211.6:c.1636_1639del	ENSP00000423828.2:p.Ser546PhefsTer2
ENST00000520401.1:c.123_126del
NM_000038.5:c.1636_1639del	NP_000029.2:p.Ser546PhefsTer2
NM_001127510.2:c.1636_1639del	NP_001120982.1:p.Ser546PhefsTer2
NM_001127511.2:c.1582_1585del	NP_001120983.2:p.Ser528PhefsTer2
NM_001354895.1:c.1636_1639del	NP_001341824.1:p.Ser546PhefsTer2
NM_001354896.1:c.1690_1693del	NP_001341825.1:p.Ser564PhefsTer2
NM_001354897.1:c.1666_1669del	NP_001341826.1:p.Ser556PhefsTer2
NM_001354898.1:c.1561_1564del	NP_001341827.1:p.Ser521PhefsTer2
NM_001354899.1:c.1552_1555del	NP_001341828.1:p.Ser518PhefsTer2
NM_001354900.1:c.1513_1516del	NP_001341829.1:p.Ser505PhefsTer2
NM_001354901.1:c.1459_1462del	NP_001341830.1:p.Ser487PhefsTer2
NM_001354902.1:c.1363_1366del	NP_001341831.1:p.Ser455PhefsTer2
NM_001354903.1:c.1333_1336del	NP_001341832.1:p.Ser445PhefsTer2
NM_001354904.1:c.1258_1261del	NP_001341833.1:p.Ser420PhefsTer2
NM_001354905.1:c.1156_1159del	NP_001341834.1:p.Ser386PhefsTer2
NM_001354906.1:c.787_790del	NP_001341835.1:p.Ser263PhefsTer2
NM_000038.6:c.1636_1639del MANE Select	NP_000029.2:p.Ser546PhefsTer2
NM_001127510.3:c.1636_1639del	NP_001120982.1:p.Ser546PhefsTer2
NM_001127511.3:c.1582_1585del	NP_001120983.2:p.Ser528PhefsTer2
NM_001354895.2:c.1636_1639del	NP_001341824.1:p.Ser546PhefsTer2
NM_001354896.2:c.1690_1693del	NP_001341825.1:p.Ser564PhefsTer2
NM_001354897.2:c.1666_1669del	NP_001341826.1:p.Ser556PhefsTer2
NM_001354898.2:c.1561_1564del	NP_001341827.1:p.Ser521PhefsTer2
NM_001354899.2:c.1552_1555del	NP_001341828.1:p.Ser518PhefsTer2
NM_001354900.2:c.1513_1516del	NP_001341829.1:p.Ser505PhefsTer2
NM_001354901.2:c.1459_1462del	NP_001341830.1:p.Ser487PhefsTer2
NM_001354902.2:c.1363_1366del	NP_001341831.1:p.Ser455PhefsTer2
NM_001354903.2:c.1333_1336del	NP_001341832.1:p.Ser445PhefsTer2
NM_001354904.2:c.1258_1261del	NP_001341833.1:p.Ser420PhefsTer2
NM_001354905.2:c.1156_1159del	NP_001341834.1:p.Ser386PhefsTer2
NM_001354906.2:c.787_790del	NP_001341835.1:p.Ser263PhefsTer2