Canonical Allele Identifier: CA2832533712

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840436_112842548del , CM000667.2:g.112840436_112842548del	GRCh38
NC_000005.9:g.112176133_112178245del , CM000667.1:g.112176133_112178245del	GRCh37
NC_000005.8:g.112204032_112206144del	NCBI36
NG_008481.4:g.152916_155028del , LRG_130:g.152916_155028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4896_7008del	ENSP00000473355.2:p.Tyr1633AspfsTer18
ENST00000505350.2:c.*4848_*6960del	ENSP00000481752.1:n.*4848_*6960del
ENST00000507379.6:c.4788_6900del	ENSP00000423224.2:p.Tyr1597AspfsTer18
ENST00000509732.6:c.4842_6954del	ENSP00000426541.2:p.Tyr1615AspfsTer18
ENST00000512211.7:c.4842_6954del	ENSP00000423828.3:p.Tyr1615AspfsTer18
ENST00000257430.9:c.4842_6954del MANE Select	ENSP00000257430.4:p.Tyr1615AspfsTer18
ENST00000257430.8:c.4842_6954del	ENSP00000257430.4:p.Tyr1615AspfsTer18
ENST00000508376.6:c.4842_6954del	ENSP00000427089.2:p.Tyr1615AspfsTer18
ENST00000508624.5:c.*4164_*6276del	ENSP00000424265.1:n.*4164_*6276del
ENST00000520401.1:c.230+11464_230+13576del
NM_000038.5:c.4842_6954del	NP_000029.2:p.Tyr1615AspfsTer18
NM_001127510.2:c.4842_6954del	NP_001120982.1:p.Tyr1615AspfsTer18
NM_001127511.2:c.4788_6900del	NP_001120983.2:p.Tyr1597AspfsTer18
NM_001354895.1:c.4842_6954del	NP_001341824.1:p.Tyr1615AspfsTer18
NM_001354896.1:c.4896_7008del	NP_001341825.1:p.Tyr1633AspfsTer18
NM_001354897.1:c.4872_6984del	NP_001341826.1:p.Tyr1625AspfsTer18
NM_001354898.1:c.4767_6879del	NP_001341827.1:p.Tyr1590AspfsTer18
NM_001354899.1:c.4758_6870del	NP_001341828.1:p.Tyr1587AspfsTer18
NM_001354900.1:c.4719_6831del	NP_001341829.1:p.Tyr1574AspfsTer18
NM_001354901.1:c.4665_6777del	NP_001341830.1:p.Tyr1556AspfsTer18
NM_001354902.1:c.4569_6681del	NP_001341831.1:p.Tyr1524AspfsTer18
NM_001354903.1:c.4539_6651del	NP_001341832.1:p.Tyr1514AspfsTer18
NM_001354904.1:c.4464_6576del	NP_001341833.1:p.Tyr1489AspfsTer18
NM_001354905.1:c.4362_6474del	NP_001341834.1:p.Tyr1455AspfsTer18
NM_001354906.1:c.3993_6105del	NP_001341835.1:p.Tyr1332AspfsTer18
NM_000038.6:c.4842_6954del MANE Select	NP_000029.2:p.Tyr1615AspfsTer18
NM_001127510.3:c.4842_6954del	NP_001120982.1:p.Tyr1615AspfsTer18
NM_001127511.3:c.4788_6900del	NP_001120983.2:p.Tyr1597AspfsTer18
NM_001354895.2:c.4842_6954del	NP_001341824.1:p.Tyr1615AspfsTer18
NM_001354896.2:c.4896_7008del	NP_001341825.1:p.Tyr1633AspfsTer18
NM_001354897.2:c.4872_6984del	NP_001341826.1:p.Tyr1625AspfsTer18
NM_001354898.2:c.4767_6879del	NP_001341827.1:p.Tyr1590AspfsTer18
NM_001354899.2:c.4758_6870del	NP_001341828.1:p.Tyr1587AspfsTer18
NM_001354900.2:c.4719_6831del	NP_001341829.1:p.Tyr1574AspfsTer18
NM_001354901.2:c.4665_6777del	NP_001341830.1:p.Tyr1556AspfsTer18
NM_001354902.2:c.4569_6681del	NP_001341831.1:p.Tyr1524AspfsTer18
NM_001354903.2:c.4539_6651del	NP_001341832.1:p.Tyr1514AspfsTer18
NM_001354904.2:c.4464_6576del	NP_001341833.1:p.Tyr1489AspfsTer18
NM_001354905.2:c.4362_6474del	NP_001341834.1:p.Tyr1455AspfsTer18
NM_001354906.2:c.3993_6105del	NP_001341835.1:p.Tyr1332AspfsTer18