Canonical Allele Identifier: CA1573472306
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840490_112840491delinsTA , CM000667.2:g.112840490_112840491delinsTA GRCh38
NC_000005.9:g.112176187_112176188delinsTA , CM000667.1:g.112176187_112176188delinsTA GRCh37
NC_000005.8:g.112204086_112204087delinsTA NCBI36
NG_008481.4:g.152970_152971delinsTA , LRG_130:g.152970_152971delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.4950_4951delinsTA ENSP00000473355.2:p.Phe1650=
ENST00000505350.2:c.*4902_*4903delinsTA ENSP00000481752.1:n.*4902_*4903delinsTA
ENST00000507379.6:c.4842_4843delinsTA ENSP00000423224.2:p.Phe1614=
ENST00000509732.6:c.4896_4897delinsTA ENSP00000426541.2:p.Phe1632=
ENST00000512211.7:c.4896_4897delinsTA ENSP00000423828.3:p.Phe1632=
ENST00000257430.9:c.4896_4897delinsTA MANE Select ENSP00000257430.4:p.Phe1632=
ENST00000257430.8:c.4896_4897delinsTA ENSP00000257430.4:p.Phe1632=
ENST00000508376.6:c.4896_4897delinsTA ENSP00000427089.2:p.Phe1632=
ENST00000508624.5:c.*4218_*4219delinsTA ENSP00000424265.1:n.*4218_*4219delinsTA
ENST00000520401.1:c.230+11518_230+11519delinsTA
NM_000038.5:c.4896_4897delinsTA NP_000029.2:p.Phe1632=
NM_001127510.2:c.4896_4897delinsTA NP_001120982.1:p.Phe1632=
NM_001127511.2:c.4842_4843delinsTA NP_001120983.2:p.Phe1614=
NM_001354895.1:c.4896_4897delinsTA NP_001341824.1:p.Phe1632=
NM_001354896.1:c.4950_4951delinsTA NP_001341825.1:p.Phe1650=
NM_001354897.1:c.4926_4927delinsTA NP_001341826.1:p.Phe1642=
NM_001354898.1:c.4821_4822delinsTA NP_001341827.1:p.Phe1607=
NM_001354899.1:c.4812_4813delinsTA NP_001341828.1:p.Phe1604=
NM_001354900.1:c.4773_4774delinsTA NP_001341829.1:p.Phe1591=
NM_001354901.1:c.4719_4720delinsTA NP_001341830.1:p.Phe1573=
NM_001354902.1:c.4623_4624delinsTA NP_001341831.1:p.Phe1541=
NM_001354903.1:c.4593_4594delinsTA NP_001341832.1:p.Phe1531=
NM_001354904.1:c.4518_4519delinsTA NP_001341833.1:p.Phe1506=
NM_001354905.1:c.4416_4417delinsTA NP_001341834.1:p.Phe1472=
NM_001354906.1:c.4047_4048delinsTA NP_001341835.1:p.Phe1349=
NM_000038.6:c.4896_4897delinsTA MANE Select NP_000029.2:p.Phe1632=
NM_001127510.3:c.4896_4897delinsTA NP_001120982.1:p.Phe1632=
NM_001127511.3:c.4842_4843delinsTA NP_001120983.2:p.Phe1614=
NM_001354895.2:c.4896_4897delinsTA NP_001341824.1:p.Phe1632=
NM_001354896.2:c.4950_4951delinsTA NP_001341825.1:p.Phe1650=
NM_001354897.2:c.4926_4927delinsTA NP_001341826.1:p.Phe1642=
NM_001354898.2:c.4821_4822delinsTA NP_001341827.1:p.Phe1607=
NM_001354899.2:c.4812_4813delinsTA NP_001341828.1:p.Phe1604=
NM_001354900.2:c.4773_4774delinsTA NP_001341829.1:p.Phe1591=
NM_001354901.2:c.4719_4720delinsTA NP_001341830.1:p.Phe1573=
NM_001354902.2:c.4623_4624delinsTA NP_001341831.1:p.Phe1541=
NM_001354903.2:c.4593_4594delinsTA NP_001341832.1:p.Phe1531=
NM_001354904.2:c.4518_4519delinsTA NP_001341833.1:p.Phe1506=
NM_001354905.2:c.4416_4417delinsTA NP_001341834.1:p.Phe1472=
NM_001354906.2:c.4047_4048delinsTA NP_001341835.1:p.Phe1349=