Canonical Allele Identifier: CA2695205301

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840260_112840261delinsT , CM000667.2:g.112840260_112840261delinsT	GRCh38
NC_000005.9:g.112175957_112175958delinsT , CM000667.1:g.112175957_112175958delinsT	GRCh37
NC_000005.8:g.112203856_112203857delinsT	NCBI36
NG_008481.4:g.152740_152741delinsT , LRG_130:g.152740_152741delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4720_4721delinsT	ENSP00000473355.2:p.Thr1574LeufsTer9
ENST00000505350.2:c.*4672_*4673delinsT	ENSP00000481752.1:n.*4672_*4673delinsT
ENST00000507379.6:c.4612_4613delinsT	ENSP00000423224.2:p.Thr1538LeufsTer9
ENST00000509732.6:c.4666_4667delinsT	ENSP00000426541.2:p.Thr1556LeufsTer9
ENST00000512211.7:c.4666_4667delinsT	ENSP00000423828.3:p.Thr1556LeufsTer9
ENST00000257430.9:c.4666_4667delinsT MANE Select	ENSP00000257430.4:p.Thr1556LeufsTer9
ENST00000257430.8:c.4666_4667delinsT	ENSP00000257430.4:p.Thr1556LeufsTer9
ENST00000508376.6:c.4666_4667delinsT	ENSP00000427089.2:p.Thr1556LeufsTer9
ENST00000508624.5:c.*3988_*3989delinsT	ENSP00000424265.1:n.*3988_*3989delinsT
ENST00000520401.1:c.230+11288_230+11289delinsT
NM_000038.5:c.4666_4667delinsT	NP_000029.2:p.Thr1556LeufsTer9
NM_001127510.2:c.4666_4667delinsT	NP_001120982.1:p.Thr1556LeufsTer9
NM_001127511.2:c.4612_4613delinsT	NP_001120983.2:p.Thr1538LeufsTer9
NM_001354895.1:c.4666_4667delinsT	NP_001341824.1:p.Thr1556LeufsTer9
NM_001354896.1:c.4720_4721delinsT	NP_001341825.1:p.Thr1574LeufsTer9
NM_001354897.1:c.4696_4697delinsT	NP_001341826.1:p.Thr1566LeufsTer9
NM_001354898.1:c.4591_4592delinsT	NP_001341827.1:p.Thr1531LeufsTer9
NM_001354899.1:c.4582_4583delinsT	NP_001341828.1:p.Thr1528LeufsTer9
NM_001354900.1:c.4543_4544delinsT	NP_001341829.1:p.Thr1515LeufsTer9
NM_001354901.1:c.4489_4490delinsT	NP_001341830.1:p.Thr1497LeufsTer9
NM_001354902.1:c.4393_4394delinsT	NP_001341831.1:p.Thr1465LeufsTer9
NM_001354903.1:c.4363_4364delinsT	NP_001341832.1:p.Thr1455LeufsTer9
NM_001354904.1:c.4288_4289delinsT	NP_001341833.1:p.Thr1430LeufsTer9
NM_001354905.1:c.4186_4187delinsT	NP_001341834.1:p.Thr1396LeufsTer9
NM_001354906.1:c.3817_3818delinsT	NP_001341835.1:p.Thr1273LeufsTer9
NM_000038.6:c.4666_4667delinsT MANE Select	NP_000029.2:p.Thr1556LeufsTer9
NM_001127510.3:c.4666_4667delinsT	NP_001120982.1:p.Thr1556LeufsTer9
NM_001127511.3:c.4612_4613delinsT	NP_001120983.2:p.Thr1538LeufsTer9
NM_001354895.2:c.4666_4667delinsT	NP_001341824.1:p.Thr1556LeufsTer9
NM_001354896.2:c.4720_4721delinsT	NP_001341825.1:p.Thr1574LeufsTer9
NM_001354897.2:c.4696_4697delinsT	NP_001341826.1:p.Thr1566LeufsTer9
NM_001354898.2:c.4591_4592delinsT	NP_001341827.1:p.Thr1531LeufsTer9
NM_001354899.2:c.4582_4583delinsT	NP_001341828.1:p.Thr1528LeufsTer9
NM_001354900.2:c.4543_4544delinsT	NP_001341829.1:p.Thr1515LeufsTer9
NM_001354901.2:c.4489_4490delinsT	NP_001341830.1:p.Thr1497LeufsTer9
NM_001354902.2:c.4393_4394delinsT	NP_001341831.1:p.Thr1465LeufsTer9
NM_001354903.2:c.4363_4364delinsT	NP_001341832.1:p.Thr1455LeufsTer9
NM_001354904.2:c.4288_4289delinsT	NP_001341833.1:p.Thr1430LeufsTer9
NM_001354905.2:c.4186_4187delinsT	NP_001341834.1:p.Thr1396LeufsTer9
NM_001354906.2:c.3817_3818delinsT	NP_001341835.1:p.Thr1273LeufsTer9