Canonical Allele Identifier: CA1573491125

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839505_112839508delinsTAGC , CM000667.2:g.112839505_112839508delinsTAGC	GRCh38
NC_000005.9:g.112175202_112175205delinsTAGC , CM000667.1:g.112175202_112175205delinsTAGC	GRCh37
NC_000005.8:g.112203101_112203104delinsTAGC	NCBI36
NG_008481.4:g.151985_151988delinsTAGC , LRG_130:g.151985_151988delinsTAGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3576_3579delinsTAGC	ENSP00000484935.2:n.3576_3579delinsTAGC
ENST00000504915.3:c.3965_3968delinsTAGC	ENSP00000473355.2:p.Ile1322=
ENST00000505350.2:c.*3917_*3920delinsTAGC	ENSP00000481752.1:n.*3917_*3920delinsTAGC...
ENST00000507379.6:c.3857_3860delinsTAGC	ENSP00000423224.2:p.Ile1286=
ENST00000509732.6:c.3911_3914delinsTAGC	ENSP00000426541.2:p.Ile1304=
ENST00000512211.7:c.3911_3914delinsTAGC	ENSP00000423828.3:p.Ile1304=
ENST00000257430.9:c.3911_3914delinsTAGC MANE Select	ENSP00000257430.4:p.Ile1304=
ENST00000257430.8:c.3911_3914delinsTAGC	ENSP00000257430.4:p.Ile1304=
ENST00000502371.2:c.2264_2267delinsTAGC
ENST00000508376.6:c.3911_3914delinsTAGC	ENSP00000427089.2:p.Ile1304=
ENST00000508624.5:c.*3233_*3236delinsTAGC	ENSP00000424265.1:n.*3233_*3236delinsTAGC...
ENST00000512211.6:c.3911_3914delinsTAGC	ENSP00000423828.2:p.Ile1304=
ENST00000520401.1:c.230+10533_230+10536delinsTAGC
NM_000038.5:c.3911_3914delinsTAGC	NP_000029.2:p.Ile1304=
NM_001127510.2:c.3911_3914delinsTAGC	NP_001120982.1:p.Ile1304=
NM_001127511.2:c.3857_3860delinsTAGC	NP_001120983.2:p.Ile1286=
NM_001354895.1:c.3911_3914delinsTAGC	NP_001341824.1:p.Ile1304=
NM_001354896.1:c.3965_3968delinsTAGC	NP_001341825.1:p.Ile1322=
NM_001354897.1:c.3941_3944delinsTAGC	NP_001341826.1:p.Ile1314=
NM_001354898.1:c.3836_3839delinsTAGC	NP_001341827.1:p.Ile1279=
NM_001354899.1:c.3827_3830delinsTAGC	NP_001341828.1:p.Ile1276=
NM_001354900.1:c.3788_3791delinsTAGC	NP_001341829.1:p.Ile1263=
NM_001354901.1:c.3734_3737delinsTAGC	NP_001341830.1:p.Ile1245=
NM_001354902.1:c.3638_3641delinsTAGC	NP_001341831.1:p.Ile1213=
NM_001354903.1:c.3608_3611delinsTAGC	NP_001341832.1:p.Ile1203=
NM_001354904.1:c.3533_3536delinsTAGC	NP_001341833.1:p.Ile1178=
NM_001354905.1:c.3431_3434delinsTAGC	NP_001341834.1:p.Ile1144=
NM_001354906.1:c.3062_3065delinsTAGC	NP_001341835.1:p.Ile1021=
NM_000038.6:c.3911_3914delinsTAGC MANE Select	NP_000029.2:p.Ile1304=
NM_001127510.3:c.3911_3914delinsTAGC	NP_001120982.1:p.Ile1304=
NM_001127511.3:c.3857_3860delinsTAGC	NP_001120983.2:p.Ile1286=
NM_001354895.2:c.3911_3914delinsTAGC	NP_001341824.1:p.Ile1304=
NM_001354896.2:c.3965_3968delinsTAGC	NP_001341825.1:p.Ile1322=
NM_001354897.2:c.3941_3944delinsTAGC	NP_001341826.1:p.Ile1314=
NM_001354898.2:c.3836_3839delinsTAGC	NP_001341827.1:p.Ile1279=
NM_001354899.2:c.3827_3830delinsTAGC	NP_001341828.1:p.Ile1276=
NM_001354900.2:c.3788_3791delinsTAGC	NP_001341829.1:p.Ile1263=
NM_001354901.2:c.3734_3737delinsTAGC	NP_001341830.1:p.Ile1245=
NM_001354902.2:c.3638_3641delinsTAGC	NP_001341831.1:p.Ile1213=
NM_001354903.2:c.3608_3611delinsTAGC	NP_001341832.1:p.Ile1203=
NM_001354904.2:c.3533_3536delinsTAGC	NP_001341833.1:p.Ile1178=
NM_001354905.2:c.3431_3434delinsTAGC	NP_001341834.1:p.Ile1144=
NM_001354906.2:c.3062_3065delinsTAGC	NP_001341835.1:p.Ile1021=