Canonical Allele Identifier: CA2739273278

Gene: APC

Linked Data

• ClinVar Variation Id: 2894799
• ClinVar RCV Id: RCV003650267

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840162_112840164del , CM000667.2:g.112840162_112840164del	GRCh38
NC_000005.9:g.112175859_112175861del , CM000667.1:g.112175859_112175861del	GRCh37
NC_000005.8:g.112203758_112203760del	NCBI36
NG_008481.4:g.152642_152644del , LRG_130:g.152642_152644del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4622_4624del	ENSP00000473355.2:p.Arg1541del
ENST00000505350.2:c.*4574_*4576del	ENSP00000481752.1:n.*4574_*4576del
ENST00000507379.6:c.4514_4516del	ENSP00000423224.2:p.Arg1505del
ENST00000509732.6:c.4568_4570del	ENSP00000426541.2:p.Arg1523del
ENST00000512211.7:c.4568_4570del	ENSP00000423828.3:p.Arg1523del
ENST00000257430.9:c.4568_4570del MANE Select	ENSP00000257430.4:p.Arg1523del
ENST00000257430.8:c.4568_4570del	ENSP00000257430.4:p.Arg1523del
ENST00000508376.6:c.4568_4570del	ENSP00000427089.2:p.Arg1523del
ENST00000508624.5:c.*3890_*3892del	ENSP00000424265.1:n.*3890_*3892del
ENST00000520401.1:c.230+11190_230+11192del
NM_000038.5:c.4568_4570del	NP_000029.2:p.Arg1523del
NM_001127510.2:c.4568_4570del	NP_001120982.1:p.Arg1523del
NM_001127511.2:c.4514_4516del	NP_001120983.2:p.Arg1505del
NM_001354895.1:c.4568_4570del	NP_001341824.1:p.Arg1523del
NM_001354896.1:c.4622_4624del	NP_001341825.1:p.Arg1541del
NM_001354897.1:c.4598_4600del	NP_001341826.1:p.Arg1533del
NM_001354898.1:c.4493_4495del	NP_001341827.1:p.Arg1498del
NM_001354899.1:c.4484_4486del	NP_001341828.1:p.Arg1495del
NM_001354900.1:c.4445_4447del	NP_001341829.1:p.Arg1482del
NM_001354901.1:c.4391_4393del	NP_001341830.1:p.Arg1464del
NM_001354902.1:c.4295_4297del	NP_001341831.1:p.Arg1432del
NM_001354903.1:c.4265_4267del	NP_001341832.1:p.Arg1422del
NM_001354904.1:c.4190_4192del	NP_001341833.1:p.Arg1397del
NM_001354905.1:c.4088_4090del	NP_001341834.1:p.Arg1363del
NM_001354906.1:c.3719_3721del	NP_001341835.1:p.Arg1240del
NM_000038.6:c.4568_4570del MANE Select	NP_000029.2:p.Arg1523del
NM_001127510.3:c.4568_4570del	NP_001120982.1:p.Arg1523del
NM_001127511.3:c.4514_4516del	NP_001120983.2:p.Arg1505del
NM_001354895.2:c.4568_4570del	NP_001341824.1:p.Arg1523del
NM_001354896.2:c.4622_4624del	NP_001341825.1:p.Arg1541del
NM_001354897.2:c.4598_4600del	NP_001341826.1:p.Arg1533del
NM_001354898.2:c.4493_4495del	NP_001341827.1:p.Arg1498del
NM_001354899.2:c.4484_4486del	NP_001341828.1:p.Arg1495del
NM_001354900.2:c.4445_4447del	NP_001341829.1:p.Arg1482del
NM_001354901.2:c.4391_4393del	NP_001341830.1:p.Arg1464del
NM_001354902.2:c.4295_4297del	NP_001341831.1:p.Arg1432del
NM_001354903.2:c.4265_4267del	NP_001341832.1:p.Arg1422del
NM_001354904.2:c.4190_4192del	NP_001341833.1:p.Arg1397del
NM_001354905.2:c.4088_4090del	NP_001341834.1:p.Arg1363del
NM_001354906.2:c.3719_3721del	NP_001341835.1:p.Arg1240del