Canonical Allele Identifier: CA1573473000
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840596_112840600delinsGAGTT , CM000667.2:g.112840596_112840600delinsGAGTT GRCh38
NC_000005.9:g.112176293_112176297delinsGAGTT , CM000667.1:g.112176293_112176297delinsGAGTT GRCh37
NC_000005.8:g.112204192_112204196delinsGAGTT NCBI36
NG_008481.4:g.153076_153080delinsGAGTT , LRG_130:g.153076_153080delinsGAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.5056_5060delinsGAGTT ENSP00000473355.2:p.Glu1686=
ENST00000505350.2:c.*5008_*5012delinsGAGTT ENSP00000481752.1:n.*5008_*5012delinsGAGTT
ENST00000507379.6:c.4948_4952delinsGAGTT ENSP00000423224.2:p.Glu1650=
ENST00000509732.6:c.5002_5006delinsGAGTT ENSP00000426541.2:p.Glu1668=
ENST00000512211.7:c.5002_5006delinsGAGTT ENSP00000423828.3:p.Glu1668=
ENST00000257430.9:c.5002_5006delinsGAGTT MANE Select ENSP00000257430.4:p.Glu1668=
ENST00000257430.8:c.5002_5006delinsGAGTT ENSP00000257430.4:p.Glu1668=
ENST00000508376.6:c.5002_5006delinsGAGTT ENSP00000427089.2:p.Glu1668=
ENST00000508624.5:c.*4324_*4328delinsGAGTT ENSP00000424265.1:n.*4324_*4328delinsGAGTT
ENST00000520401.1:c.230+11624_230+11628delinsGAGTT
NM_000038.5:c.5002_5006delinsGAGTT NP_000029.2:p.Glu1668=
NM_001127510.2:c.5002_5006delinsGAGTT NP_001120982.1:p.Glu1668=
NM_001127511.2:c.4948_4952delinsGAGTT NP_001120983.2:p.Glu1650=
NM_001354895.1:c.5002_5006delinsGAGTT NP_001341824.1:p.Glu1668=
NM_001354896.1:c.5056_5060delinsGAGTT NP_001341825.1:p.Glu1686=
NM_001354897.1:c.5032_5036delinsGAGTT NP_001341826.1:p.Glu1678=
NM_001354898.1:c.4927_4931delinsGAGTT NP_001341827.1:p.Glu1643=
NM_001354899.1:c.4918_4922delinsGAGTT NP_001341828.1:p.Glu1640=
NM_001354900.1:c.4879_4883delinsGAGTT NP_001341829.1:p.Glu1627=
NM_001354901.1:c.4825_4829delinsGAGTT NP_001341830.1:p.Glu1609=
NM_001354902.1:c.4729_4733delinsGAGTT NP_001341831.1:p.Glu1577=
NM_001354903.1:c.4699_4703delinsGAGTT NP_001341832.1:p.Glu1567=
NM_001354904.1:c.4624_4628delinsGAGTT NP_001341833.1:p.Glu1542=
NM_001354905.1:c.4522_4526delinsGAGTT NP_001341834.1:p.Glu1508=
NM_001354906.1:c.4153_4157delinsGAGTT NP_001341835.1:p.Glu1385=
NM_000038.6:c.5002_5006delinsGAGTT MANE Select NP_000029.2:p.Glu1668=
NM_001127510.3:c.5002_5006delinsGAGTT NP_001120982.1:p.Glu1668=
NM_001127511.3:c.4948_4952delinsGAGTT NP_001120983.2:p.Glu1650=
NM_001354895.2:c.5002_5006delinsGAGTT NP_001341824.1:p.Glu1668=
NM_001354896.2:c.5056_5060delinsGAGTT NP_001341825.1:p.Glu1686=
NM_001354897.2:c.5032_5036delinsGAGTT NP_001341826.1:p.Glu1678=
NM_001354898.2:c.4927_4931delinsGAGTT NP_001341827.1:p.Glu1643=
NM_001354899.2:c.4918_4922delinsGAGTT NP_001341828.1:p.Glu1640=
NM_001354900.2:c.4879_4883delinsGAGTT NP_001341829.1:p.Glu1627=
NM_001354901.2:c.4825_4829delinsGAGTT NP_001341830.1:p.Glu1609=
NM_001354902.2:c.4729_4733delinsGAGTT NP_001341831.1:p.Glu1577=
NM_001354903.2:c.4699_4703delinsGAGTT NP_001341832.1:p.Glu1567=
NM_001354904.2:c.4624_4628delinsGAGTT NP_001341833.1:p.Glu1542=
NM_001354905.2:c.4522_4526delinsGAGTT NP_001341834.1:p.Glu1508=
NM_001354906.2:c.4153_4157delinsGAGTT NP_001341835.1:p.Glu1385=