Canonical Allele Identifier: CA010742
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112841438_112841439delinsGGAAAA , CM000667.2:g.112841438_112841439delinsGGAAAA GRCh38
NC_000005.9:g.112177135_112177136delinsGGAAAA , CM000667.1:g.112177135_112177136delinsGGAAAA GRCh37
NC_000005.8:g.112205034_112205035delinsGGAAAA NCBI36
NG_008481.4:g.153918_153919delinsGGAAAA , LRG_130:g.153918_153919delinsGGAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.5898_5899delinsGGAAAA ENSP00000473355.2:p.Asp1966GlufsTer11
ENST00000505350.2:c.*5850_*5851delinsGGAAAA ENSP00000481752.1:n.*5850_*5851delinsGGAAAA
ENST00000507379.6:c.5790_5791delinsGGAAAA ENSP00000423224.2:p.Asp1930GlufsTer11
ENST00000509732.6:c.5844_5845delinsGGAAAA ENSP00000426541.2:p.Asp1948GlufsTer11
ENST00000512211.7:c.5844_5845delinsGGAAAA ENSP00000423828.3:p.Asp1948GlufsTer11
ENST00000257430.9:c.5844_5845delinsGGAAAA MANE Select ENSP00000257430.4:p.Asp1948GlufsTer11
ENST00000257430.8:c.5844_5845delinsGGAAAA ENSP00000257430.4:p.Asp1948GlufsTer11
ENST00000508376.6:c.5844_5845delinsGGAAAA ENSP00000427089.2:p.Asp1948GlufsTer11
ENST00000508624.5:c.*5166_*5167delinsGGAAAA ENSP00000424265.1:n.*5166_*5167delinsGGAAAA
ENST00000520401.1:c.230+12466_230+12467delinsGGAAAA
NM_000038.5:c.5844_5845delinsGGAAAA NP_000029.2:p.Asp1948GlufsTer11
NM_001127510.2:c.5844_5845delinsGGAAAA NP_001120982.1:p.Asp1948GlufsTer11
NM_001127511.2:c.5790_5791delinsGGAAAA NP_001120983.2:p.Asp1930GlufsTer11
NM_001354895.1:c.5844_5845delinsGGAAAA NP_001341824.1:p.Asp1948GlufsTer11
NM_001354896.1:c.5898_5899delinsGGAAAA NP_001341825.1:p.Asp1966GlufsTer11
NM_001354897.1:c.5874_5875delinsGGAAAA NP_001341826.1:p.Asp1958GlufsTer11
NM_001354898.1:c.5769_5770delinsGGAAAA NP_001341827.1:p.Asp1923GlufsTer11
NM_001354899.1:c.5760_5761delinsGGAAAA NP_001341828.1:p.Asp1920GlufsTer11
NM_001354900.1:c.5721_5722delinsGGAAAA NP_001341829.1:p.Asp1907GlufsTer11
NM_001354901.1:c.5667_5668delinsGGAAAA NP_001341830.1:p.Asp1889GlufsTer11
NM_001354902.1:c.5571_5572delinsGGAAAA NP_001341831.1:p.Asp1857GlufsTer11
NM_001354903.1:c.5541_5542delinsGGAAAA NP_001341832.1:p.Asp1847GlufsTer11
NM_001354904.1:c.5466_5467delinsGGAAAA NP_001341833.1:p.Asp1822GlufsTer11
NM_001354905.1:c.5364_5365delinsGGAAAA NP_001341834.1:p.Asp1788GlufsTer11
NM_001354906.1:c.4995_4996delinsGGAAAA NP_001341835.1:p.Asp1665GlufsTer11
NM_000038.6:c.5844_5845delinsGGAAAA MANE Select NP_000029.2:p.Asp1948GlufsTer11
NM_001127510.3:c.5844_5845delinsGGAAAA NP_001120982.1:p.Asp1948GlufsTer11
NM_001127511.3:c.5790_5791delinsGGAAAA NP_001120983.2:p.Asp1930GlufsTer11
NM_001354895.2:c.5844_5845delinsGGAAAA NP_001341824.1:p.Asp1948GlufsTer11
NM_001354896.2:c.5898_5899delinsGGAAAA NP_001341825.1:p.Asp1966GlufsTer11
NM_001354897.2:c.5874_5875delinsGGAAAA NP_001341826.1:p.Asp1958GlufsTer11
NM_001354898.2:c.5769_5770delinsGGAAAA NP_001341827.1:p.Asp1923GlufsTer11
NM_001354899.2:c.5760_5761delinsGGAAAA NP_001341828.1:p.Asp1920GlufsTer11
NM_001354900.2:c.5721_5722delinsGGAAAA NP_001341829.1:p.Asp1907GlufsTer11
NM_001354901.2:c.5667_5668delinsGGAAAA NP_001341830.1:p.Asp1889GlufsTer11
NM_001354902.2:c.5571_5572delinsGGAAAA NP_001341831.1:p.Asp1857GlufsTer11
NM_001354903.2:c.5541_5542delinsGGAAAA NP_001341832.1:p.Asp1847GlufsTer11
NM_001354904.2:c.5466_5467delinsGGAAAA NP_001341833.1:p.Asp1822GlufsTer11
NM_001354905.2:c.5364_5365delinsGGAAAA NP_001341834.1:p.Asp1788GlufsTer11
NM_001354906.2:c.4995_4996delinsGGAAAA NP_001341835.1:p.Asp1665GlufsTer11