Canonical Allele Identifier: CA445963858
Gene: APC HGNC NCBI

Linked Data

COSMIC: COSM19581
MyVariant Identifiers: chr5:g.112175199del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112839504del , CM000667.2:g.112839504del GRCh38
NC_000005.9:g.112175201del , CM000667.1:g.112175201del GRCh37
NC_000005.8:g.112203100del NCBI36
NG_008481.4:g.151984del , LRG_130:g.151984del

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.3575del ENSP00000484935.2:n.3575del
ENST00000504915.3:c.3964del ENSP00000473355.2:p.Ile1322Ter
ENST00000505350.2:c.*3916del ENSP00000481752.1:n.*3916del
ENST00000507379.6:c.3856del ENSP00000423224.2:p.Ile1286Ter
ENST00000509732.6:c.3910del ENSP00000426541.2:p.Ile1304Ter
ENST00000512211.7:c.3910del ENSP00000423828.3:p.Ile1304Ter
ENST00000257430.9:c.3910del MANE Select ENSP00000257430.4:p.Ile1304Ter
ENST00000257430.8:c.3910del ENSP00000257430.4:p.Ile1304Ter
ENST00000502371.2:c.2263del
ENST00000508376.6:c.3910del ENSP00000427089.2:p.Ile1304Ter
ENST00000508624.5:c.*3232del ENSP00000424265.1:n.*3232del
ENST00000512211.6:c.3910del ENSP00000423828.2:p.Ile1304Ter
ENST00000520401.1:c.230+10532del
NM_000038.5:c.3910del NP_000029.2:p.Ile1304Ter
NM_001127510.2:c.3910del NP_001120982.1:p.Ile1304Ter
NM_001127511.2:c.3856del NP_001120983.2:p.Ile1286Ter
NM_001354895.1:c.3910del NP_001341824.1:p.Ile1304Ter
NM_001354896.1:c.3964del NP_001341825.1:p.Ile1322Ter
NM_001354897.1:c.3940del NP_001341826.1:p.Ile1314Ter
NM_001354898.1:c.3835del NP_001341827.1:p.Ile1279Ter
NM_001354899.1:c.3826del NP_001341828.1:p.Ile1276Ter
NM_001354900.1:c.3787del NP_001341829.1:p.Ile1263Ter
NM_001354901.1:c.3733del NP_001341830.1:p.Ile1245Ter
NM_001354902.1:c.3637del NP_001341831.1:p.Ile1213Ter
NM_001354903.1:c.3607del NP_001341832.1:p.Ile1203Ter
NM_001354904.1:c.3532del NP_001341833.1:p.Ile1178Ter
NM_001354905.1:c.3430del NP_001341834.1:p.Ile1144Ter
NM_001354906.1:c.3061del NP_001341835.1:p.Ile1021Ter
NM_000038.6:c.3910del MANE Select NP_000029.2:p.Ile1304Ter
NM_001127510.3:c.3910del NP_001120982.1:p.Ile1304Ter
NM_001127511.3:c.3856del NP_001120983.2:p.Ile1286Ter
NM_001354895.2:c.3910del NP_001341824.1:p.Ile1304Ter
NM_001354896.2:c.3964del NP_001341825.1:p.Ile1322Ter
NM_001354897.2:c.3940del NP_001341826.1:p.Ile1314Ter
NM_001354898.2:c.3835del NP_001341827.1:p.Ile1279Ter
NM_001354899.2:c.3826del NP_001341828.1:p.Ile1276Ter
NM_001354900.2:c.3787del NP_001341829.1:p.Ile1263Ter
NM_001354901.2:c.3733del NP_001341830.1:p.Ile1245Ter
NM_001354902.2:c.3637del NP_001341831.1:p.Ile1213Ter
NM_001354903.2:c.3607del NP_001341832.1:p.Ile1203Ter
NM_001354904.2:c.3532del NP_001341833.1:p.Ile1178Ter
NM_001354905.2:c.3430del NP_001341834.1:p.Ile1144Ter
NM_001354906.2:c.3061del NP_001341835.1:p.Ile1021Ter