Canonical Allele Identifier: CA1573471025

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835068_112835069delinsAC , CM000667.2:g.112835068_112835069delinsAC	GRCh38
NC_000005.9:g.112170765_112170766delinsAC , CM000667.1:g.112170765_112170766delinsAC	GRCh37
NC_000005.8:g.112198664_112198665delinsAC	NCBI36
NG_008481.4:g.147548_147549delinsAC , LRG_130:g.147548_147549delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1526_1527delinsAC	ENSP00000484935.2:n.1526_1527delinsAC
ENST00000504915.3:c.1915_1916delinsAC	ENSP00000473355.2:p.Thr639=
ENST00000505350.2:c.*1867_*1868delinsAC	ENSP00000481752.1:n.*1867_*1868delinsAC
ENST00000507379.6:c.1807_1808delinsAC	ENSP00000423224.2:p.Thr603=
ENST00000509732.6:c.1861_1862delinsAC	ENSP00000426541.2:p.Thr621=
ENST00000512211.7:c.1861_1862delinsAC	ENSP00000423828.3:p.Thr621=
ENST00000257430.9:c.1861_1862delinsAC MANE Select	ENSP00000257430.4:p.Thr621=
ENST00000257430.8:c.1861_1862delinsAC	ENSP00000257430.4:p.Thr621=
ENST00000502371.2:c.214_215delinsAC
ENST00000504915.2:c.550_551delinsAC	ENSP00000473355.1:p.Thr184=
ENST00000507379.5:c.1807_1808delinsAC	ENSP00000423224.1:p.Thr603=
ENST00000508376.6:c.1861_1862delinsAC	ENSP00000427089.2:p.Thr621=
ENST00000508624.5:c.*1183_*1184delinsAC	ENSP00000424265.1:n.*1183_*1184delinsAC
ENST00000512211.6:c.1861_1862delinsAC	ENSP00000423828.2:p.Thr621=
ENST00000520401.1:c.230+6096_230+6097delinsAC
NM_000038.5:c.1861_1862delinsAC	NP_000029.2:p.Thr621=
NM_001127510.2:c.1861_1862delinsAC	NP_001120982.1:p.Thr621=
NM_001127511.2:c.1807_1808delinsAC	NP_001120983.2:p.Thr603=
NM_001354895.1:c.1861_1862delinsAC	NP_001341824.1:p.Thr621=
NM_001354896.1:c.1915_1916delinsAC	NP_001341825.1:p.Thr639=
NM_001354897.1:c.1891_1892delinsAC	NP_001341826.1:p.Thr631=
NM_001354898.1:c.1786_1787delinsAC	NP_001341827.1:p.Thr596=
NM_001354899.1:c.1777_1778delinsAC	NP_001341828.1:p.Thr593=
NM_001354900.1:c.1738_1739delinsAC	NP_001341829.1:p.Thr580=
NM_001354901.1:c.1684_1685delinsAC	NP_001341830.1:p.Thr562=
NM_001354902.1:c.1588_1589delinsAC	NP_001341831.1:p.Thr530=
NM_001354903.1:c.1558_1559delinsAC	NP_001341832.1:p.Thr520=
NM_001354904.1:c.1483_1484delinsAC	NP_001341833.1:p.Thr495=
NM_001354905.1:c.1381_1382delinsAC	NP_001341834.1:p.Thr461=
NM_001354906.1:c.1012_1013delinsAC	NP_001341835.1:p.Thr338=
NM_000038.6:c.1861_1862delinsAC MANE Select	NP_000029.2:p.Thr621=
NM_001127510.3:c.1861_1862delinsAC	NP_001120982.1:p.Thr621=
NM_001127511.3:c.1807_1808delinsAC	NP_001120983.2:p.Thr603=
NM_001354895.2:c.1861_1862delinsAC	NP_001341824.1:p.Thr621=
NM_001354896.2:c.1915_1916delinsAC	NP_001341825.1:p.Thr639=
NM_001354897.2:c.1891_1892delinsAC	NP_001341826.1:p.Thr631=
NM_001354898.2:c.1786_1787delinsAC	NP_001341827.1:p.Thr596=
NM_001354899.2:c.1777_1778delinsAC	NP_001341828.1:p.Thr593=
NM_001354900.2:c.1738_1739delinsAC	NP_001341829.1:p.Thr580=
NM_001354901.2:c.1684_1685delinsAC	NP_001341830.1:p.Thr562=
NM_001354902.2:c.1588_1589delinsAC	NP_001341831.1:p.Thr530=
NM_001354903.2:c.1558_1559delinsAC	NP_001341832.1:p.Thr520=
NM_001354904.2:c.1483_1484delinsAC	NP_001341833.1:p.Thr495=
NM_001354905.2:c.1381_1382delinsAC	NP_001341834.1:p.Thr461=
NM_001354906.2:c.1012_1013delinsAC	NP_001341835.1:p.Thr338=