Canonical Allele Identifier: CA1573486140

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838715_112838717delinsCAA , CM000667.2:g.112838715_112838717delinsCAA	GRCh38
NC_000005.9:g.112174412_112174414delinsCAA , CM000667.1:g.112174412_112174414delinsCAA	GRCh37
NC_000005.8:g.112202311_112202313delinsCAA	NCBI36
NG_008481.4:g.151195_151197delinsCAA , LRG_130:g.151195_151197delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2786_2788delinsCAA	ENSP00000484935.2:n.2786_2788delinsCAA
ENST00000504915.3:c.3175_3177delinsCAA	ENSP00000473355.2:p.Gln1059=
ENST00000505350.2:c.*3127_*3129delinsCAA	ENSP00000481752.1:n.*3127_*3129delinsCAA
ENST00000507379.6:c.3067_3069delinsCAA	ENSP00000423224.2:p.Gln1023=
ENST00000509732.6:c.3121_3123delinsCAA	ENSP00000426541.2:p.Gln1041=
ENST00000512211.7:c.3121_3123delinsCAA	ENSP00000423828.3:p.Gln1041=
ENST00000257430.9:c.3121_3123delinsCAA MANE Select	ENSP00000257430.4:p.Gln1041=
ENST00000257430.8:c.3121_3123delinsCAA	ENSP00000257430.4:p.Gln1041=
ENST00000502371.2:c.1474_1476delinsCAA
ENST00000507379.5:c.3067_3069delinsCAA	ENSP00000423224.1:p.Gln1023=
ENST00000508376.6:c.3121_3123delinsCAA	ENSP00000427089.2:p.Gln1041=
ENST00000508624.5:c.*2443_*2445delinsCAA	ENSP00000424265.1:n.*2443_*2445delinsCAA
ENST00000512211.6:c.3121_3123delinsCAA	ENSP00000423828.2:p.Gln1041=
ENST00000520401.1:c.230+9743_230+9745delinsCAA
NM_000038.5:c.3121_3123delinsCAA	NP_000029.2:p.Gln1041=
NM_001127510.2:c.3121_3123delinsCAA	NP_001120982.1:p.Gln1041=
NM_001127511.2:c.3067_3069delinsCAA	NP_001120983.2:p.Gln1023=
NM_001354895.1:c.3121_3123delinsCAA	NP_001341824.1:p.Gln1041=
NM_001354896.1:c.3175_3177delinsCAA	NP_001341825.1:p.Gln1059=
NM_001354897.1:c.3151_3153delinsCAA	NP_001341826.1:p.Gln1051=
NM_001354898.1:c.3046_3048delinsCAA	NP_001341827.1:p.Gln1016=
NM_001354899.1:c.3037_3039delinsCAA	NP_001341828.1:p.Gln1013=
NM_001354900.1:c.2998_3000delinsCAA	NP_001341829.1:p.Gln1000=
NM_001354901.1:c.2944_2946delinsCAA	NP_001341830.1:p.Gln982=
NM_001354902.1:c.2848_2850delinsCAA	NP_001341831.1:p.Gln950=
NM_001354903.1:c.2818_2820delinsCAA	NP_001341832.1:p.Gln940=
NM_001354904.1:c.2743_2745delinsCAA	NP_001341833.1:p.Gln915=
NM_001354905.1:c.2641_2643delinsCAA	NP_001341834.1:p.Gln881=
NM_001354906.1:c.2272_2274delinsCAA	NP_001341835.1:p.Gln758=
NM_000038.6:c.3121_3123delinsCAA MANE Select	NP_000029.2:p.Gln1041=
NM_001127510.3:c.3121_3123delinsCAA	NP_001120982.1:p.Gln1041=
NM_001127511.3:c.3067_3069delinsCAA	NP_001120983.2:p.Gln1023=
NM_001354895.2:c.3121_3123delinsCAA	NP_001341824.1:p.Gln1041=
NM_001354896.2:c.3175_3177delinsCAA	NP_001341825.1:p.Gln1059=
NM_001354897.2:c.3151_3153delinsCAA	NP_001341826.1:p.Gln1051=
NM_001354898.2:c.3046_3048delinsCAA	NP_001341827.1:p.Gln1016=
NM_001354899.2:c.3037_3039delinsCAA	NP_001341828.1:p.Gln1013=
NM_001354900.2:c.2998_3000delinsCAA	NP_001341829.1:p.Gln1000=
NM_001354901.2:c.2944_2946delinsCAA	NP_001341830.1:p.Gln982=
NM_001354902.2:c.2848_2850delinsCAA	NP_001341831.1:p.Gln950=
NM_001354903.2:c.2818_2820delinsCAA	NP_001341832.1:p.Gln940=
NM_001354904.2:c.2743_2745delinsCAA	NP_001341833.1:p.Gln915=
NM_001354905.2:c.2641_2643delinsCAA	NP_001341834.1:p.Gln881=
NM_001354906.2:c.2272_2274delinsCAA	NP_001341835.1:p.Gln758=