Canonical Allele Identifier: CA445963866

Gene: APC

Linked Data

• COSMIC: COSM23582
• MyVariant Identifiers: chr5:g.112175203del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839506del , CM000667.2:g.112839506del	GRCh38
NC_000005.9:g.112175203del , CM000667.1:g.112175203del	GRCh37
NC_000005.8:g.112203102del	NCBI36
NG_008481.4:g.151986del , LRG_130:g.151986del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3577del	ENSP00000484935.2:n.3577del
ENST00000504915.3:c.3966del	ENSP00000473355.2:p.Ile1322MetfsTer4
ENST00000505350.2:c.*3918del	ENSP00000481752.1:n.*3918del
ENST00000507379.6:c.3858del	ENSP00000423224.2:p.Ile1286MetfsTer4
ENST00000509732.6:c.3912del	ENSP00000426541.2:p.Ile1304MetfsTer4
ENST00000512211.7:c.3912del	ENSP00000423828.3:p.Ile1304MetfsTer4
ENST00000257430.9:c.3912del MANE Select	ENSP00000257430.4:p.Ile1304MetfsTer4
ENST00000257430.8:c.3912del	ENSP00000257430.4:p.Ile1304MetfsTer4
ENST00000502371.2:c.2265del
ENST00000508376.6:c.3912del	ENSP00000427089.2:p.Ile1304MetfsTer4
ENST00000508624.5:c.*3234del	ENSP00000424265.1:n.*3234del
ENST00000512211.6:c.3912del	ENSP00000423828.2:p.Ile1304MetfsTer?
ENST00000520401.1:c.230+10534del
NM_000038.5:c.3912del	NP_000029.2:p.Ile1304MetfsTer4
NM_001127510.2:c.3912del	NP_001120982.1:p.Ile1304MetfsTer4
NM_001127511.2:c.3858del	NP_001120983.2:p.Ile1286MetfsTer4
NM_001354895.1:c.3912del	NP_001341824.1:p.Ile1304MetfsTer4
NM_001354896.1:c.3966del	NP_001341825.1:p.Ile1322MetfsTer4
NM_001354897.1:c.3942del	NP_001341826.1:p.Ile1314MetfsTer4
NM_001354898.1:c.3837del	NP_001341827.1:p.Ile1279MetfsTer4
NM_001354899.1:c.3828del	NP_001341828.1:p.Ile1276MetfsTer4
NM_001354900.1:c.3789del	NP_001341829.1:p.Ile1263MetfsTer4
NM_001354901.1:c.3735del	NP_001341830.1:p.Ile1245MetfsTer4
NM_001354902.1:c.3639del	NP_001341831.1:p.Ile1213MetfsTer4
NM_001354903.1:c.3609del	NP_001341832.1:p.Ile1203MetfsTer4
NM_001354904.1:c.3534del	NP_001341833.1:p.Ile1178MetfsTer4
NM_001354905.1:c.3432del	NP_001341834.1:p.Ile1144MetfsTer4
NM_001354906.1:c.3063del	NP_001341835.1:p.Ile1021MetfsTer4
NM_000038.6:c.3912del MANE Select	NP_000029.2:p.Ile1304MetfsTer4
NM_001127510.3:c.3912del	NP_001120982.1:p.Ile1304MetfsTer4
NM_001127511.3:c.3858del	NP_001120983.2:p.Ile1286MetfsTer4
NM_001354895.2:c.3912del	NP_001341824.1:p.Ile1304MetfsTer4
NM_001354896.2:c.3966del	NP_001341825.1:p.Ile1322MetfsTer4
NM_001354897.2:c.3942del	NP_001341826.1:p.Ile1314MetfsTer4
NM_001354898.2:c.3837del	NP_001341827.1:p.Ile1279MetfsTer4
NM_001354899.2:c.3828del	NP_001341828.1:p.Ile1276MetfsTer4
NM_001354900.2:c.3789del	NP_001341829.1:p.Ile1263MetfsTer4
NM_001354901.2:c.3735del	NP_001341830.1:p.Ile1245MetfsTer4
NM_001354902.2:c.3639del	NP_001341831.1:p.Ile1213MetfsTer4
NM_001354903.2:c.3609del	NP_001341832.1:p.Ile1203MetfsTer4
NM_001354904.2:c.3534del	NP_001341833.1:p.Ile1178MetfsTer4
NM_001354905.2:c.3432del	NP_001341834.1:p.Ile1144MetfsTer4
NM_001354906.2:c.3063del	NP_001341835.1:p.Ile1021MetfsTer4