Canonical Allele Identifier: CA1573470346

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112834957_112834958delinsAC , CM000667.2:g.112834957_112834958delinsAC	GRCh38
NC_000005.9:g.112170654_112170655delinsAC , CM000667.1:g.112170654_112170655delinsAC	GRCh37
NC_000005.8:g.112198553_112198554delinsAC	NCBI36
NG_008481.4:g.147437_147438delinsAC , LRG_130:g.147437_147438delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1415_1416delinsAC	ENSP00000484935.2:p.Asn472=
ENST00000504915.3:c.1804_1805delinsAC	ENSP00000473355.2:p.Thr602=
ENST00000505350.2:c.*1756_*1757delinsAC	ENSP00000481752.1:n.*1756_*1757delinsAC
ENST00000507379.6:c.1696_1697delinsAC	ENSP00000423224.2:p.Thr566=
ENST00000509732.6:c.1750_1751delinsAC	ENSP00000426541.2:p.Thr584=
ENST00000512211.7:c.1750_1751delinsAC	ENSP00000423828.3:p.Thr584=
ENST00000257430.9:c.1750_1751delinsAC MANE Select	ENSP00000257430.4:p.Thr584=
ENST00000257430.8:c.1750_1751delinsAC	ENSP00000257430.4:p.Thr584=
ENST00000502371.2:c.103_104delinsAC
ENST00000504915.2:c.439_440delinsAC	ENSP00000473355.1:p.Thr147=
ENST00000507379.5:c.1696_1697delinsAC	ENSP00000423224.1:p.Thr566=
ENST00000508376.6:c.1750_1751delinsAC	ENSP00000427089.2:p.Thr584=
ENST00000508624.5:c.*1072_*1073delinsAC	ENSP00000424265.1:n.*1072_*1073delinsAC
ENST00000512211.6:c.1750_1751delinsAC	ENSP00000423828.2:p.Thr584=
ENST00000520401.1:c.230+5985_230+5986delinsAC
NM_000038.5:c.1750_1751delinsAC	NP_000029.2:p.Thr584=
NM_001127510.2:c.1750_1751delinsAC	NP_001120982.1:p.Thr584=
NM_001127511.2:c.1696_1697delinsAC	NP_001120983.2:p.Thr566=
NM_001354895.1:c.1750_1751delinsAC	NP_001341824.1:p.Thr584=
NM_001354896.1:c.1804_1805delinsAC	NP_001341825.1:p.Thr602=
NM_001354897.1:c.1780_1781delinsAC	NP_001341826.1:p.Thr594=
NM_001354898.1:c.1675_1676delinsAC	NP_001341827.1:p.Thr559=
NM_001354899.1:c.1666_1667delinsAC	NP_001341828.1:p.Thr556=
NM_001354900.1:c.1627_1628delinsAC	NP_001341829.1:p.Thr543=
NM_001354901.1:c.1573_1574delinsAC	NP_001341830.1:p.Thr525=
NM_001354902.1:c.1477_1478delinsAC	NP_001341831.1:p.Thr493=
NM_001354903.1:c.1447_1448delinsAC	NP_001341832.1:p.Thr483=
NM_001354904.1:c.1372_1373delinsAC	NP_001341833.1:p.Thr458=
NM_001354905.1:c.1270_1271delinsAC	NP_001341834.1:p.Thr424=
NM_001354906.1:c.901_902delinsAC	NP_001341835.1:p.Thr301=
NM_000038.6:c.1750_1751delinsAC MANE Select	NP_000029.2:p.Thr584=
NM_001127510.3:c.1750_1751delinsAC	NP_001120982.1:p.Thr584=
NM_001127511.3:c.1696_1697delinsAC	NP_001120983.2:p.Thr566=
NM_001354895.2:c.1750_1751delinsAC	NP_001341824.1:p.Thr584=
NM_001354896.2:c.1804_1805delinsAC	NP_001341825.1:p.Thr602=
NM_001354897.2:c.1780_1781delinsAC	NP_001341826.1:p.Thr594=
NM_001354898.2:c.1675_1676delinsAC	NP_001341827.1:p.Thr559=
NM_001354899.2:c.1666_1667delinsAC	NP_001341828.1:p.Thr556=
NM_001354900.2:c.1627_1628delinsAC	NP_001341829.1:p.Thr543=
NM_001354901.2:c.1573_1574delinsAC	NP_001341830.1:p.Thr525=
NM_001354902.2:c.1477_1478delinsAC	NP_001341831.1:p.Thr493=
NM_001354903.2:c.1447_1448delinsAC	NP_001341832.1:p.Thr483=
NM_001354904.2:c.1372_1373delinsAC	NP_001341833.1:p.Thr458=
NM_001354905.2:c.1270_1271delinsAC	NP_001341834.1:p.Thr424=
NM_001354906.2:c.901_902delinsAC	NP_001341835.1:p.Thr301=