Canonical Allele Identifier: CA2710001260

Gene: APC

Linked Data

• dbSNP Id: rs2149921354

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840293_112840307del , CM000667.2:g.112840293_112840307del	GRCh38
NC_000005.9:g.112175990_112176004del , CM000667.1:g.112175990_112176004del	GRCh37
NC_000005.8:g.112203889_112203903del	NCBI36
NG_008481.4:g.152773_152787del , LRG_130:g.152773_152787del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4753_4767del	ENSP00000473355.2:p.Ser1585_Asp1589del
ENST00000505350.2:c.*4705_*4719del	ENSP00000481752.1:n.*4705_*4719del
ENST00000507379.6:c.4645_4659del	ENSP00000423224.2:p.Ser1549_Asp1553del
ENST00000509732.6:c.4699_4713del	ENSP00000426541.2:p.Ser1567_Asp1571del
ENST00000512211.7:c.4699_4713del	ENSP00000423828.3:p.Ser1567_Asp1571del
ENST00000257430.9:c.4699_4713del MANE Select	ENSP00000257430.4:p.Ser1567_Asp1571del
ENST00000257430.8:c.4699_4713del	ENSP00000257430.4:p.Ser1567_Asp1571del
ENST00000508376.6:c.4699_4713del	ENSP00000427089.2:p.Ser1567_Asp1571del
ENST00000508624.5:c.*4021_*4035del	ENSP00000424265.1:n.*4021_*4035del
ENST00000520401.1:c.230+11321_230+11335del
NM_000038.5:c.4699_4713del	NP_000029.2:p.Ser1567_Asp1571del
NM_001127510.2:c.4699_4713del	NP_001120982.1:p.Ser1567_Asp1571del
NM_001127511.2:c.4645_4659del	NP_001120983.2:p.Ser1549_Asp1553del
NM_001354895.1:c.4699_4713del	NP_001341824.1:p.Ser1567_Asp1571del
NM_001354896.1:c.4753_4767del	NP_001341825.1:p.Ser1585_Asp1589del
NM_001354897.1:c.4729_4743del	NP_001341826.1:p.Ser1577_Asp1581del
NM_001354898.1:c.4624_4638del	NP_001341827.1:p.Ser1542_Asp1546del
NM_001354899.1:c.4615_4629del	NP_001341828.1:p.Ser1539_Asp1543del
NM_001354900.1:c.4576_4590del	NP_001341829.1:p.Ser1526_Asp1530del
NM_001354901.1:c.4522_4536del	NP_001341830.1:p.Ser1508_Asp1512del
NM_001354902.1:c.4426_4440del	NP_001341831.1:p.Ser1476_Asp1480del
NM_001354903.1:c.4396_4410del	NP_001341832.1:p.Ser1466_Asp1470del
NM_001354904.1:c.4321_4335del	NP_001341833.1:p.Ser1441_Asp1445del
NM_001354905.1:c.4219_4233del	NP_001341834.1:p.Ser1407_Asp1411del
NM_001354906.1:c.3850_3864del	NP_001341835.1:p.Ser1284_Asp1288del
NM_000038.6:c.4699_4713del MANE Select	NP_000029.2:p.Ser1567_Asp1571del
NM_001127510.3:c.4699_4713del	NP_001120982.1:p.Ser1567_Asp1571del
NM_001127511.3:c.4645_4659del	NP_001120983.2:p.Ser1549_Asp1553del
NM_001354895.2:c.4699_4713del	NP_001341824.1:p.Ser1567_Asp1571del
NM_001354896.2:c.4753_4767del	NP_001341825.1:p.Ser1585_Asp1589del
NM_001354897.2:c.4729_4743del	NP_001341826.1:p.Ser1577_Asp1581del
NM_001354898.2:c.4624_4638del	NP_001341827.1:p.Ser1542_Asp1546del
NM_001354899.2:c.4615_4629del	NP_001341828.1:p.Ser1539_Asp1543del
NM_001354900.2:c.4576_4590del	NP_001341829.1:p.Ser1526_Asp1530del
NM_001354901.2:c.4522_4536del	NP_001341830.1:p.Ser1508_Asp1512del
NM_001354902.2:c.4426_4440del	NP_001341831.1:p.Ser1476_Asp1480del
NM_001354903.2:c.4396_4410del	NP_001341832.1:p.Ser1466_Asp1470del
NM_001354904.2:c.4321_4335del	NP_001341833.1:p.Ser1441_Asp1445del
NM_001354905.2:c.4219_4233del	NP_001341834.1:p.Ser1407_Asp1411del
NM_001354906.2:c.3850_3864del	NP_001341835.1:p.Ser1284_Asp1288del