Canonical Allele Identifier: CA1573470694

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840263_112840264delinsAT , CM000667.2:g.112840263_112840264delinsAT	GRCh38
NC_000005.9:g.112175960_112175961delinsAT , CM000667.1:g.112175960_112175961delinsAT	GRCh37
NC_000005.8:g.112203859_112203860delinsAT	NCBI36
NG_008481.4:g.152743_152744delinsAT , LRG_130:g.152743_152744delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4723_4724delinsAT	ENSP00000473355.2:p.Ile1575=
ENST00000505350.2:c.*4675_*4676delinsAT	ENSP00000481752.1:n.*4675_*4676delinsAT
ENST00000507379.6:c.4615_4616delinsAT	ENSP00000423224.2:p.Ile1539=
ENST00000509732.6:c.4669_4670delinsAT	ENSP00000426541.2:p.Ile1557=
ENST00000512211.7:c.4669_4670delinsAT	ENSP00000423828.3:p.Ile1557=
ENST00000257430.9:c.4669_4670delinsAT MANE Select	ENSP00000257430.4:p.Ile1557=
ENST00000257430.8:c.4669_4670delinsAT	ENSP00000257430.4:p.Ile1557=
ENST00000508376.6:c.4669_4670delinsAT	ENSP00000427089.2:p.Ile1557=
ENST00000508624.5:c.*3991_*3992delinsAT	ENSP00000424265.1:n.*3991_*3992delinsAT
ENST00000520401.1:c.230+11291_230+11292delinsAT
NM_000038.5:c.4669_4670delinsAT	NP_000029.2:p.Ile1557=
NM_001127510.2:c.4669_4670delinsAT	NP_001120982.1:p.Ile1557=
NM_001127511.2:c.4615_4616delinsAT	NP_001120983.2:p.Ile1539=
NM_001354895.1:c.4669_4670delinsAT	NP_001341824.1:p.Ile1557=
NM_001354896.1:c.4723_4724delinsAT	NP_001341825.1:p.Ile1575=
NM_001354897.1:c.4699_4700delinsAT	NP_001341826.1:p.Ile1567=
NM_001354898.1:c.4594_4595delinsAT	NP_001341827.1:p.Ile1532=
NM_001354899.1:c.4585_4586delinsAT	NP_001341828.1:p.Ile1529=
NM_001354900.1:c.4546_4547delinsAT	NP_001341829.1:p.Ile1516=
NM_001354901.1:c.4492_4493delinsAT	NP_001341830.1:p.Ile1498=
NM_001354902.1:c.4396_4397delinsAT	NP_001341831.1:p.Ile1466=
NM_001354903.1:c.4366_4367delinsAT	NP_001341832.1:p.Ile1456=
NM_001354904.1:c.4291_4292delinsAT	NP_001341833.1:p.Ile1431=
NM_001354905.1:c.4189_4190delinsAT	NP_001341834.1:p.Ile1397=
NM_001354906.1:c.3820_3821delinsAT	NP_001341835.1:p.Ile1274=
NM_000038.6:c.4669_4670delinsAT MANE Select	NP_000029.2:p.Ile1557=
NM_001127510.3:c.4669_4670delinsAT	NP_001120982.1:p.Ile1557=
NM_001127511.3:c.4615_4616delinsAT	NP_001120983.2:p.Ile1539=
NM_001354895.2:c.4669_4670delinsAT	NP_001341824.1:p.Ile1557=
NM_001354896.2:c.4723_4724delinsAT	NP_001341825.1:p.Ile1575=
NM_001354897.2:c.4699_4700delinsAT	NP_001341826.1:p.Ile1567=
NM_001354898.2:c.4594_4595delinsAT	NP_001341827.1:p.Ile1532=
NM_001354899.2:c.4585_4586delinsAT	NP_001341828.1:p.Ile1529=
NM_001354900.2:c.4546_4547delinsAT	NP_001341829.1:p.Ile1516=
NM_001354901.2:c.4492_4493delinsAT	NP_001341830.1:p.Ile1498=
NM_001354902.2:c.4396_4397delinsAT	NP_001341831.1:p.Ile1466=
NM_001354903.2:c.4366_4367delinsAT	NP_001341832.1:p.Ile1456=
NM_001354904.2:c.4291_4292delinsAT	NP_001341833.1:p.Ile1431=
NM_001354905.2:c.4189_4190delinsAT	NP_001341834.1:p.Ile1397=
NM_001354906.2:c.3820_3821delinsAT	NP_001341835.1:p.Ile1274=