Canonical Allele Identifier: CA446206596

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112175866_112175867insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840169_112840170insA , CM000667.2:g.112840169_112840170insA	GRCh38
NC_000005.9:g.112175866_112175867insA , CM000667.1:g.112175866_112175867insA	GRCh37
NC_000005.8:g.112203765_112203766insA	NCBI36
NG_008481.4:g.152649_152650insA , LRG_130:g.152649_152650insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4629_4630insA	ENSP00000473355.2:p.Pro1544ThrfsTer7
ENST00000505350.2:c.*4581_*4582insA	ENSP00000481752.1:n.*4581_*4582insA
ENST00000507379.6:c.4521_4522insA	ENSP00000423224.2:p.Pro1508ThrfsTer7
ENST00000509732.6:c.4575_4576insA	ENSP00000426541.2:p.Pro1526ThrfsTer7
ENST00000512211.7:c.4575_4576insA	ENSP00000423828.3:p.Pro1526ThrfsTer7
ENST00000257430.9:c.4575_4576insA MANE Select	ENSP00000257430.4:p.Pro1526ThrfsTer7
ENST00000257430.8:c.4575_4576insA	ENSP00000257430.4:p.Pro1526ThrfsTer7
ENST00000508376.6:c.4575_4576insA	ENSP00000427089.2:p.Pro1526ThrfsTer7
ENST00000508624.5:c.*3897_*3898insA	ENSP00000424265.1:n.*3897_*3898insA
ENST00000520401.1:c.230+11197_230+11198insA
NM_000038.5:c.4575_4576insA	NP_000029.2:p.Pro1526ThrfsTer7
NM_001127510.2:c.4575_4576insA	NP_001120982.1:p.Pro1526ThrfsTer7
NM_001127511.2:c.4521_4522insA	NP_001120983.2:p.Pro1508ThrfsTer7
NM_001354895.1:c.4575_4576insA	NP_001341824.1:p.Pro1526ThrfsTer7
NM_001354896.1:c.4629_4630insA	NP_001341825.1:p.Pro1544ThrfsTer7
NM_001354897.1:c.4605_4606insA	NP_001341826.1:p.Pro1536ThrfsTer7
NM_001354898.1:c.4500_4501insA	NP_001341827.1:p.Pro1501ThrfsTer7
NM_001354899.1:c.4491_4492insA	NP_001341828.1:p.Pro1498ThrfsTer7
NM_001354900.1:c.4452_4453insA	NP_001341829.1:p.Pro1485ThrfsTer7
NM_001354901.1:c.4398_4399insA	NP_001341830.1:p.Pro1467ThrfsTer7
NM_001354902.1:c.4302_4303insA	NP_001341831.1:p.Pro1435ThrfsTer7
NM_001354903.1:c.4272_4273insA	NP_001341832.1:p.Pro1425ThrfsTer7
NM_001354904.1:c.4197_4198insA	NP_001341833.1:p.Pro1400ThrfsTer7
NM_001354905.1:c.4095_4096insA	NP_001341834.1:p.Pro1366ThrfsTer7
NM_001354906.1:c.3726_3727insA	NP_001341835.1:p.Pro1243ThrfsTer7
NM_000038.6:c.4575_4576insA MANE Select	NP_000029.2:p.Pro1526ThrfsTer7
NM_001127510.3:c.4575_4576insA	NP_001120982.1:p.Pro1526ThrfsTer7
NM_001127511.3:c.4521_4522insA	NP_001120983.2:p.Pro1508ThrfsTer7
NM_001354895.2:c.4575_4576insA	NP_001341824.1:p.Pro1526ThrfsTer7
NM_001354896.2:c.4629_4630insA	NP_001341825.1:p.Pro1544ThrfsTer7
NM_001354897.2:c.4605_4606insA	NP_001341826.1:p.Pro1536ThrfsTer7
NM_001354898.2:c.4500_4501insA	NP_001341827.1:p.Pro1501ThrfsTer7
NM_001354899.2:c.4491_4492insA	NP_001341828.1:p.Pro1498ThrfsTer7
NM_001354900.2:c.4452_4453insA	NP_001341829.1:p.Pro1485ThrfsTer7
NM_001354901.2:c.4398_4399insA	NP_001341830.1:p.Pro1467ThrfsTer7
NM_001354902.2:c.4302_4303insA	NP_001341831.1:p.Pro1435ThrfsTer7
NM_001354903.2:c.4272_4273insA	NP_001341832.1:p.Pro1425ThrfsTer7
NM_001354904.2:c.4197_4198insA	NP_001341833.1:p.Pro1400ThrfsTer7
NM_001354905.2:c.4095_4096insA	NP_001341834.1:p.Pro1366ThrfsTer7
NM_001354906.2:c.3726_3727insA	NP_001341835.1:p.Pro1243ThrfsTer7