Canonical Allele Identifier: CA658760794

Gene: APC

Linked Data

• PubMed: PMID:20223039

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840576_112840577insTA , CM000667.2:g.112840576_112840577insTA	GRCh38
NC_000005.9:g.112176273_112176274insTA , CM000667.1:g.112176273_112176274insTA	GRCh37
NC_000005.8:g.112204172_112204173insTA	NCBI36
NG_008481.4:g.153056_153057insTA , LRG_130:g.153056_153057insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5036_5037insTA	ENSP00000473355.2:p.Ile1680LysfsTer9
ENST00000505350.2:c.*4988_*4989insTA	ENSP00000481752.1:n.*4988_*4989insTA
ENST00000507379.6:c.4928_4929insTA	ENSP00000423224.2:p.Ile1644LysfsTer9
ENST00000509732.6:c.4982_4983insTA	ENSP00000426541.2:p.Ile1662LysfsTer9
ENST00000512211.7:c.4982_4983insTA	ENSP00000423828.3:p.Ile1662LysfsTer9
ENST00000257430.9:c.4982_4983insTA MANE Select	ENSP00000257430.4:p.Ile1662LysfsTer9
ENST00000257430.8:c.4982_4983insTA	ENSP00000257430.4:p.Ile1662LysfsTer9
ENST00000508376.6:c.4982_4983insTA	ENSP00000427089.2:p.Ile1662LysfsTer9
ENST00000508624.5:c.*4304_*4305insTA	ENSP00000424265.1:n.*4304_*4305insTA
ENST00000520401.1:c.230+11604_230+11605insTA
NM_000038.5:c.4982_4983insTA	NP_000029.2:p.Ile1662LysfsTer9
NM_001127510.2:c.4982_4983insTA	NP_001120982.1:p.Ile1662LysfsTer9
NM_001127511.2:c.4928_4929insTA	NP_001120983.2:p.Ile1644LysfsTer9
NM_001354895.1:c.4982_4983insTA	NP_001341824.1:p.Ile1662LysfsTer9
NM_001354896.1:c.5036_5037insTA	NP_001341825.1:p.Ile1680LysfsTer9
NM_001354897.1:c.5012_5013insTA	NP_001341826.1:p.Ile1672LysfsTer9
NM_001354898.1:c.4907_4908insTA	NP_001341827.1:p.Ile1637LysfsTer9
NM_001354899.1:c.4898_4899insTA	NP_001341828.1:p.Ile1634LysfsTer9
NM_001354900.1:c.4859_4860insTA	NP_001341829.1:p.Ile1621LysfsTer9
NM_001354901.1:c.4805_4806insTA	NP_001341830.1:p.Ile1603LysfsTer9
NM_001354902.1:c.4709_4710insTA	NP_001341831.1:p.Ile1571LysfsTer9
NM_001354903.1:c.4679_4680insTA	NP_001341832.1:p.Ile1561LysfsTer9
NM_001354904.1:c.4604_4605insTA	NP_001341833.1:p.Ile1536LysfsTer9
NM_001354905.1:c.4502_4503insTA	NP_001341834.1:p.Ile1502LysfsTer9
NM_001354906.1:c.4133_4134insTA	NP_001341835.1:p.Ile1379LysfsTer9
NM_000038.6:c.4982_4983insTA MANE Select	NP_000029.2:p.Ile1662LysfsTer9
NM_001127510.3:c.4982_4983insTA	NP_001120982.1:p.Ile1662LysfsTer9
NM_001127511.3:c.4928_4929insTA	NP_001120983.2:p.Ile1644LysfsTer9
NM_001354895.2:c.4982_4983insTA	NP_001341824.1:p.Ile1662LysfsTer9
NM_001354896.2:c.5036_5037insTA	NP_001341825.1:p.Ile1680LysfsTer9
NM_001354897.2:c.5012_5013insTA	NP_001341826.1:p.Ile1672LysfsTer9
NM_001354898.2:c.4907_4908insTA	NP_001341827.1:p.Ile1637LysfsTer9
NM_001354899.2:c.4898_4899insTA	NP_001341828.1:p.Ile1634LysfsTer9
NM_001354900.2:c.4859_4860insTA	NP_001341829.1:p.Ile1621LysfsTer9
NM_001354901.2:c.4805_4806insTA	NP_001341830.1:p.Ile1603LysfsTer9
NM_001354902.2:c.4709_4710insTA	NP_001341831.1:p.Ile1571LysfsTer9
NM_001354903.2:c.4679_4680insTA	NP_001341832.1:p.Ile1561LysfsTer9
NM_001354904.2:c.4604_4605insTA	NP_001341833.1:p.Ile1536LysfsTer9
NM_001354905.2:c.4502_4503insTA	NP_001341834.1:p.Ile1502LysfsTer9
NM_001354906.2:c.4133_4134insTA	NP_001341835.1:p.Ile1379LysfsTer9