Canonical Allele Identifier: CA2695198722

Gene: APC

Linked Data

• ClinVar Variation Id: 2677340
• ClinVar RCV Id: RCV003471587

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840386_112840395del , CM000667.2:g.112840386_112840395del	GRCh38
NC_000005.9:g.112176083_112176092del , CM000667.1:g.112176083_112176092del	GRCh37
NC_000005.8:g.112203982_112203991del	NCBI36
NG_008481.4:g.152866_152875del , LRG_130:g.152866_152875del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4846_4855del	ENSP00000473355.2:p.Ala1616TyrfsTer?
ENST00000505350.2:c.*4798_*4807del	ENSP00000481752.1:n.*4798_*4807del
ENST00000507379.6:c.4738_4747del	ENSP00000423224.2:p.Ala1580TyrfsTer?
ENST00000509732.6:c.4792_4801del	ENSP00000426541.2:p.Ala1598TyrfsTer?
ENST00000512211.7:c.4792_4801del	ENSP00000423828.3:p.Ala1598TyrfsTer?
ENST00000257430.9:c.4792_4801del MANE Select	ENSP00000257430.4:p.Ala1598TyrfsTer?
ENST00000257430.8:c.4792_4801del	ENSP00000257430.4:p.Ala1598TyrfsTer?
ENST00000508376.6:c.4792_4801del	ENSP00000427089.2:p.Ala1598TyrfsTer?
ENST00000508624.5:c.*4114_*4123del	ENSP00000424265.1:n.*4114_*4123del
ENST00000520401.1:c.230+11414_230+11423del
NM_000038.5:c.4792_4801del	NP_000029.2:p.Ala1598TyrfsTer?
NM_001127510.2:c.4792_4801del	NP_001120982.1:p.Ala1598TyrfsTer?
NM_001127511.2:c.4738_4747del	NP_001120983.2:p.Ala1580TyrfsTer?
NM_001354895.1:c.4792_4801del	NP_001341824.1:p.Ala1598TyrfsTer?
NM_001354896.1:c.4846_4855del	NP_001341825.1:p.Ala1616TyrfsTer?
NM_001354897.1:c.4822_4831del	NP_001341826.1:p.Ala1608TyrfsTer?
NM_001354898.1:c.4717_4726del	NP_001341827.1:p.Ala1573TyrfsTer?
NM_001354899.1:c.4708_4717del	NP_001341828.1:p.Ala1570TyrfsTer?
NM_001354900.1:c.4669_4678del	NP_001341829.1:p.Ala1557TyrfsTer?
NM_001354901.1:c.4615_4624del	NP_001341830.1:p.Ala1539TyrfsTer?
NM_001354902.1:c.4519_4528del	NP_001341831.1:p.Ala1507TyrfsTer?
NM_001354903.1:c.4489_4498del	NP_001341832.1:p.Ala1497TyrfsTer?
NM_001354904.1:c.4414_4423del	NP_001341833.1:p.Ala1472TyrfsTer?
NM_001354905.1:c.4312_4321del	NP_001341834.1:p.Ala1438TyrfsTer?
NM_001354906.1:c.3943_3952del	NP_001341835.1:p.Ala1315TyrfsTer?
NM_000038.6:c.4792_4801del MANE Select	NP_000029.2:p.Ala1598TyrfsTer?
NM_001127510.3:c.4792_4801del	NP_001120982.1:p.Ala1598TyrfsTer?
NM_001127511.3:c.4738_4747del	NP_001120983.2:p.Ala1580TyrfsTer?
NM_001354895.2:c.4792_4801del	NP_001341824.1:p.Ala1598TyrfsTer?
NM_001354896.2:c.4846_4855del	NP_001341825.1:p.Ala1616TyrfsTer?
NM_001354897.2:c.4822_4831del	NP_001341826.1:p.Ala1608TyrfsTer?
NM_001354898.2:c.4717_4726del	NP_001341827.1:p.Ala1573TyrfsTer?
NM_001354899.2:c.4708_4717del	NP_001341828.1:p.Ala1570TyrfsTer?
NM_001354900.2:c.4669_4678del	NP_001341829.1:p.Ala1557TyrfsTer?
NM_001354901.2:c.4615_4624del	NP_001341830.1:p.Ala1539TyrfsTer?
NM_001354902.2:c.4519_4528del	NP_001341831.1:p.Ala1507TyrfsTer?
NM_001354903.2:c.4489_4498del	NP_001341832.1:p.Ala1497TyrfsTer?
NM_001354904.2:c.4414_4423del	NP_001341833.1:p.Ala1472TyrfsTer?
NM_001354905.2:c.4312_4321del	NP_001341834.1:p.Ala1438TyrfsTer?
NM_001354906.2:c.3943_3952del	NP_001341835.1:p.Ala1315TyrfsTer?