Canonical Allele Identifier: CA2767942013

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840692_112840693insTTTTTC , CM000667.2:g.112840692_112840693insTTTTTC	GRCh38
NC_000005.9:g.112176389_112176390insTTTTTC , CM000667.1:g.112176389_112176390insTTTTTC	GRCh37
NC_000005.8:g.112204288_112204289insTTTTTC	NCBI36
NG_008481.4:g.153172_153173insTTTTTC , LRG_130:g.153172_153173insTTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5152_5153insTTTTTC	ENSP00000473355.2:p.Ala1718delinsValPhePro
ENST00000505350.2:c.*5104_*5105insTTTTTC	ENSP00000481752.1:n.*5104_*5105insTTTTTC
ENST00000507379.6:c.5044_5045insTTTTTC	ENSP00000423224.2:p.Ala1682delinsValPhePro
ENST00000509732.6:c.5098_5099insTTTTTC	ENSP00000426541.2:p.Ala1700delinsValPhePro
ENST00000512211.7:c.5098_5099insTTTTTC	ENSP00000423828.3:p.Ala1700delinsValPhePro
ENST00000257430.9:c.5098_5099insTTTTTC MANE Select	ENSP00000257430.4:p.Ala1700delinsValPhePro
ENST00000257430.8:c.5098_5099insTTTTTC	ENSP00000257430.4:p.Ala1700delinsValPhePro
ENST00000508376.6:c.5098_5099insTTTTTC	ENSP00000427089.2:p.Ala1700delinsValPhePro
ENST00000508624.5:c.*4420_*4421insTTTTTC	ENSP00000424265.1:n.*4420_*4421insTTTTTC
ENST00000520401.1:c.230+11720_230+11721insTTTTTC
NM_000038.5:c.5098_5099insTTTTTC	NP_000029.2:p.Ala1700delinsValPhePro
NM_001127510.2:c.5098_5099insTTTTTC	NP_001120982.1:p.Ala1700delinsValPhePro
NM_001127511.2:c.5044_5045insTTTTTC	NP_001120983.2:p.Ala1682delinsValPhePro
NM_001354895.1:c.5098_5099insTTTTTC	NP_001341824.1:p.Ala1700delinsValPhePro
NM_001354896.1:c.5152_5153insTTTTTC	NP_001341825.1:p.Ala1718delinsValPhePro
NM_001354897.1:c.5128_5129insTTTTTC	NP_001341826.1:p.Ala1710delinsValPhePro
NM_001354898.1:c.5023_5024insTTTTTC	NP_001341827.1:p.Ala1675delinsValPhePro
NM_001354899.1:c.5014_5015insTTTTTC	NP_001341828.1:p.Ala1672delinsValPhePro
NM_001354900.1:c.4975_4976insTTTTTC	NP_001341829.1:p.Ala1659delinsValPhePro
NM_001354901.1:c.4921_4922insTTTTTC	NP_001341830.1:p.Ala1641delinsValPhePro
NM_001354902.1:c.4825_4826insTTTTTC	NP_001341831.1:p.Ala1609delinsValPhePro
NM_001354903.1:c.4795_4796insTTTTTC	NP_001341832.1:p.Ala1599delinsValPhePro
NM_001354904.1:c.4720_4721insTTTTTC	NP_001341833.1:p.Ala1574delinsValPhePro
NM_001354905.1:c.4618_4619insTTTTTC	NP_001341834.1:p.Ala1540delinsValPhePro
NM_001354906.1:c.4249_4250insTTTTTC	NP_001341835.1:p.Ala1417delinsValPhePro
NM_000038.6:c.5098_5099insTTTTTC MANE Select	NP_000029.2:p.Ala1700delinsValPhePro
NM_001127510.3:c.5098_5099insTTTTTC	NP_001120982.1:p.Ala1700delinsValPhePro
NM_001127511.3:c.5044_5045insTTTTTC	NP_001120983.2:p.Ala1682delinsValPhePro
NM_001354895.2:c.5098_5099insTTTTTC	NP_001341824.1:p.Ala1700delinsValPhePro
NM_001354896.2:c.5152_5153insTTTTTC	NP_001341825.1:p.Ala1718delinsValPhePro
NM_001354897.2:c.5128_5129insTTTTTC	NP_001341826.1:p.Ala1710delinsValPhePro
NM_001354898.2:c.5023_5024insTTTTTC	NP_001341827.1:p.Ala1675delinsValPhePro
NM_001354899.2:c.5014_5015insTTTTTC	NP_001341828.1:p.Ala1672delinsValPhePro
NM_001354900.2:c.4975_4976insTTTTTC	NP_001341829.1:p.Ala1659delinsValPhePro
NM_001354901.2:c.4921_4922insTTTTTC	NP_001341830.1:p.Ala1641delinsValPhePro
NM_001354902.2:c.4825_4826insTTTTTC	NP_001341831.1:p.Ala1609delinsValPhePro
NM_001354903.2:c.4795_4796insTTTTTC	NP_001341832.1:p.Ala1599delinsValPhePro
NM_001354904.2:c.4720_4721insTTTTTC	NP_001341833.1:p.Ala1574delinsValPhePro
NM_001354905.2:c.4618_4619insTTTTTC	NP_001341834.1:p.Ala1540delinsValPhePro
NM_001354906.2:c.4249_4250insTTTTTC	NP_001341835.1:p.Ala1417delinsValPhePro