Canonical Allele Identifier: CA1573470723

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835027_112835028delinsGT , CM000667.2:g.112835027_112835028delinsGT	GRCh38
NC_000005.9:g.112170724_112170725delinsGT , CM000667.1:g.112170724_112170725delinsGT	GRCh37
NC_000005.8:g.112198623_112198624delinsGT	NCBI36
NG_008481.4:g.147507_147508delinsGT , LRG_130:g.147507_147508delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1485_1486delinsGT	ENSP00000484935.2:n.1485_1486delinsGT
ENST00000504915.3:c.1874_1875delinsGT	ENSP00000473355.2:p.Cys625=
ENST00000505350.2:c.*1826_*1827delinsGT	ENSP00000481752.1:n.*1826_*1827delinsGT
ENST00000507379.6:c.1766_1767delinsGT	ENSP00000423224.2:p.Cys589=
ENST00000509732.6:c.1820_1821delinsGT	ENSP00000426541.2:p.Cys607=
ENST00000512211.7:c.1820_1821delinsGT	ENSP00000423828.3:p.Cys607=
ENST00000257430.9:c.1820_1821delinsGT MANE Select	ENSP00000257430.4:p.Cys607=
ENST00000257430.8:c.1820_1821delinsGT	ENSP00000257430.4:p.Cys607=
ENST00000502371.2:c.173_174delinsGT
ENST00000504915.2:c.509_510delinsGT	ENSP00000473355.1:p.Cys170=
ENST00000507379.5:c.1766_1767delinsGT	ENSP00000423224.1:p.Cys589=
ENST00000508376.6:c.1820_1821delinsGT	ENSP00000427089.2:p.Cys607=
ENST00000508624.5:c.*1142_*1143delinsGT	ENSP00000424265.1:n.*1142_*1143delinsGT
ENST00000512211.6:c.1820_1821delinsGT	ENSP00000423828.2:p.Cys607=
ENST00000520401.1:c.230+6055_230+6056delinsGT
NM_000038.5:c.1820_1821delinsGT	NP_000029.2:p.Cys607=
NM_001127510.2:c.1820_1821delinsGT	NP_001120982.1:p.Cys607=
NM_001127511.2:c.1766_1767delinsGT	NP_001120983.2:p.Cys589=
NM_001354895.1:c.1820_1821delinsGT	NP_001341824.1:p.Cys607=
NM_001354896.1:c.1874_1875delinsGT	NP_001341825.1:p.Cys625=
NM_001354897.1:c.1850_1851delinsGT	NP_001341826.1:p.Cys617=
NM_001354898.1:c.1745_1746delinsGT	NP_001341827.1:p.Cys582=
NM_001354899.1:c.1736_1737delinsGT	NP_001341828.1:p.Cys579=
NM_001354900.1:c.1697_1698delinsGT	NP_001341829.1:p.Cys566=
NM_001354901.1:c.1643_1644delinsGT	NP_001341830.1:p.Cys548=
NM_001354902.1:c.1547_1548delinsGT	NP_001341831.1:p.Cys516=
NM_001354903.1:c.1517_1518delinsGT	NP_001341832.1:p.Cys506=
NM_001354904.1:c.1442_1443delinsGT	NP_001341833.1:p.Cys481=
NM_001354905.1:c.1340_1341delinsGT	NP_001341834.1:p.Cys447=
NM_001354906.1:c.971_972delinsGT	NP_001341835.1:p.Cys324=
NM_000038.6:c.1820_1821delinsGT MANE Select	NP_000029.2:p.Cys607=
NM_001127510.3:c.1820_1821delinsGT	NP_001120982.1:p.Cys607=
NM_001127511.3:c.1766_1767delinsGT	NP_001120983.2:p.Cys589=
NM_001354895.2:c.1820_1821delinsGT	NP_001341824.1:p.Cys607=
NM_001354896.2:c.1874_1875delinsGT	NP_001341825.1:p.Cys625=
NM_001354897.2:c.1850_1851delinsGT	NP_001341826.1:p.Cys617=
NM_001354898.2:c.1745_1746delinsGT	NP_001341827.1:p.Cys582=
NM_001354899.2:c.1736_1737delinsGT	NP_001341828.1:p.Cys579=
NM_001354900.2:c.1697_1698delinsGT	NP_001341829.1:p.Cys566=
NM_001354901.2:c.1643_1644delinsGT	NP_001341830.1:p.Cys548=
NM_001354902.2:c.1547_1548delinsGT	NP_001341831.1:p.Cys516=
NM_001354903.2:c.1517_1518delinsGT	NP_001341832.1:p.Cys506=
NM_001354904.2:c.1442_1443delinsGT	NP_001341833.1:p.Cys481=
NM_001354905.2:c.1340_1341delinsGT	NP_001341834.1:p.Cys447=
NM_001354906.2:c.971_972delinsGT	NP_001341835.1:p.Cys324=