Canonical Allele Identifier: CA16602715

Gene: APC

Linked Data

• ClinVar Variation Id: 376267
• ClinVar RCV Id: RCV000435941
• dbSNP Id: rs1057519846
• MyVariant Identifiers: chr5:g.112175960_112175967del (hg19) ; chr5:g.112840263_112840270del (hg38)
• PubMed: PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840263_112840270del , CM000667.2:g.112840263_112840270del	GRCh38
NC_000005.9:g.112175960_112175967del , CM000667.1:g.112175960_112175967del	GRCh37
NC_000005.8:g.112203859_112203866del	NCBI36
NG_008481.4:g.152743_152750del , LRG_130:g.152743_152750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4723_4730del	ENSP00000473355.2:p.Ile1575Ter
ENST00000505350.2:c.*4675_*4682del	ENSP00000481752.1:n.*4675_*4682del
ENST00000507379.6:c.4615_4622del	ENSP00000423224.2:p.Ile1539Ter
ENST00000509732.6:c.4669_4676del	ENSP00000426541.2:p.Ile1557Ter
ENST00000512211.7:c.4669_4676del	ENSP00000423828.3:p.Ile1557Ter
ENST00000257430.9:c.4669_4676del MANE Select	ENSP00000257430.4:p.Ile1557Ter
ENST00000257430.8:c.4669_4676del	ENSP00000257430.4:p.Ile1557Ter
ENST00000508376.6:c.4669_4676del	ENSP00000427089.2:p.Ile1557Ter
ENST00000508624.5:c.*3991_*3998del	ENSP00000424265.1:n.*3991_*3998del
ENST00000520401.1:c.230+11291_230+11298del
NM_000038.5:c.4669_4676del	NP_000029.2:p.Ile1557Ter
NM_001127510.2:c.4669_4676del	NP_001120982.1:p.Ile1557Ter
NM_001127511.2:c.4615_4622del	NP_001120983.2:p.Ile1539Ter
NM_001354895.1:c.4669_4676del	NP_001341824.1:p.Ile1557Ter
NM_001354896.1:c.4723_4730del	NP_001341825.1:p.Ile1575Ter
NM_001354897.1:c.4699_4706del	NP_001341826.1:p.Ile1567Ter
NM_001354898.1:c.4594_4601del	NP_001341827.1:p.Ile1532Ter
NM_001354899.1:c.4585_4592del	NP_001341828.1:p.Ile1529Ter
NM_001354900.1:c.4546_4553del	NP_001341829.1:p.Ile1516Ter
NM_001354901.1:c.4492_4499del	NP_001341830.1:p.Ile1498Ter
NM_001354902.1:c.4396_4403del	NP_001341831.1:p.Ile1466Ter
NM_001354903.1:c.4366_4373del	NP_001341832.1:p.Ile1456Ter
NM_001354904.1:c.4291_4298del	NP_001341833.1:p.Ile1431Ter
NM_001354905.1:c.4189_4196del	NP_001341834.1:p.Ile1397Ter
NM_001354906.1:c.3820_3827del	NP_001341835.1:p.Ile1274Ter
NM_000038.6:c.4669_4676del MANE Select	NP_000029.2:p.Ile1557Ter
NM_001127510.3:c.4669_4676del	NP_001120982.1:p.Ile1557Ter
NM_001127511.3:c.4615_4622del	NP_001120983.2:p.Ile1539Ter
NM_001354895.2:c.4669_4676del	NP_001341824.1:p.Ile1557Ter
NM_001354896.2:c.4723_4730del	NP_001341825.1:p.Ile1575Ter
NM_001354897.2:c.4699_4706del	NP_001341826.1:p.Ile1567Ter
NM_001354898.2:c.4594_4601del	NP_001341827.1:p.Ile1532Ter
NM_001354899.2:c.4585_4592del	NP_001341828.1:p.Ile1529Ter
NM_001354900.2:c.4546_4553del	NP_001341829.1:p.Ile1516Ter
NM_001354901.2:c.4492_4499del	NP_001341830.1:p.Ile1498Ter
NM_001354902.2:c.4396_4403del	NP_001341831.1:p.Ile1466Ter
NM_001354903.2:c.4366_4373del	NP_001341832.1:p.Ile1456Ter
NM_001354904.2:c.4291_4298del	NP_001341833.1:p.Ile1431Ter
NM_001354905.2:c.4189_4196del	NP_001341834.1:p.Ile1397Ter
NM_001354906.2:c.3820_3827del	NP_001341835.1:p.Ile1274Ter