Canonical Allele Identifier: CA1573474090

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840738_112840739delinsAC , CM000667.2:g.112840738_112840739delinsAC	GRCh38
NC_000005.9:g.112176435_112176436delinsAC , CM000667.1:g.112176435_112176436delinsAC	GRCh37
NC_000005.8:g.112204334_112204335delinsAC	NCBI36
NG_008481.4:g.153218_153219delinsAC , LRG_130:g.153218_153219delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5198_5199delinsAC	ENSP00000473355.2:p.Asp1733=
ENST00000505350.2:c.*5150_*5151delinsAC	ENSP00000481752.1:n.*5150_*5151delinsAC
ENST00000507379.6:c.5090_5091delinsAC	ENSP00000423224.2:p.Asp1697=
ENST00000509732.6:c.5144_5145delinsAC	ENSP00000426541.2:p.Asp1715=
ENST00000512211.7:c.5144_5145delinsAC	ENSP00000423828.3:p.Asp1715=
ENST00000257430.9:c.5144_5145delinsAC MANE Select	ENSP00000257430.4:p.Asp1715=
ENST00000257430.8:c.5144_5145delinsAC	ENSP00000257430.4:p.Asp1715=
ENST00000508376.6:c.5144_5145delinsAC	ENSP00000427089.2:p.Asp1715=
ENST00000508624.5:c.*4466_*4467delinsAC	ENSP00000424265.1:n.*4466_*4467delinsAC
ENST00000520401.1:c.230+11766_230+11767delinsAC
NM_000038.5:c.5144_5145delinsAC	NP_000029.2:p.Asp1715=
NM_001127510.2:c.5144_5145delinsAC	NP_001120982.1:p.Asp1715=
NM_001127511.2:c.5090_5091delinsAC	NP_001120983.2:p.Asp1697=
NM_001354895.1:c.5144_5145delinsAC	NP_001341824.1:p.Asp1715=
NM_001354896.1:c.5198_5199delinsAC	NP_001341825.1:p.Asp1733=
NM_001354897.1:c.5174_5175delinsAC	NP_001341826.1:p.Asp1725=
NM_001354898.1:c.5069_5070delinsAC	NP_001341827.1:p.Asp1690=
NM_001354899.1:c.5060_5061delinsAC	NP_001341828.1:p.Asp1687=
NM_001354900.1:c.5021_5022delinsAC	NP_001341829.1:p.Asp1674=
NM_001354901.1:c.4967_4968delinsAC	NP_001341830.1:p.Asp1656=
NM_001354902.1:c.4871_4872delinsAC	NP_001341831.1:p.Asp1624=
NM_001354903.1:c.4841_4842delinsAC	NP_001341832.1:p.Asp1614=
NM_001354904.1:c.4766_4767delinsAC	NP_001341833.1:p.Asp1589=
NM_001354905.1:c.4664_4665delinsAC	NP_001341834.1:p.Asp1555=
NM_001354906.1:c.4295_4296delinsAC	NP_001341835.1:p.Asp1432=
NM_000038.6:c.5144_5145delinsAC MANE Select	NP_000029.2:p.Asp1715=
NM_001127510.3:c.5144_5145delinsAC	NP_001120982.1:p.Asp1715=
NM_001127511.3:c.5090_5091delinsAC	NP_001120983.2:p.Asp1697=
NM_001354895.2:c.5144_5145delinsAC	NP_001341824.1:p.Asp1715=
NM_001354896.2:c.5198_5199delinsAC	NP_001341825.1:p.Asp1733=
NM_001354897.2:c.5174_5175delinsAC	NP_001341826.1:p.Asp1725=
NM_001354898.2:c.5069_5070delinsAC	NP_001341827.1:p.Asp1690=
NM_001354899.2:c.5060_5061delinsAC	NP_001341828.1:p.Asp1687=
NM_001354900.2:c.5021_5022delinsAC	NP_001341829.1:p.Asp1674=
NM_001354901.2:c.4967_4968delinsAC	NP_001341830.1:p.Asp1656=
NM_001354902.2:c.4871_4872delinsAC	NP_001341831.1:p.Asp1624=
NM_001354903.2:c.4841_4842delinsAC	NP_001341832.1:p.Asp1614=
NM_001354904.2:c.4766_4767delinsAC	NP_001341833.1:p.Asp1589=
NM_001354905.2:c.4664_4665delinsAC	NP_001341834.1:p.Asp1555=
NM_001354906.2:c.4295_4296delinsAC	NP_001341835.1:p.Asp1432=