Canonical Allele Identifier: CA2695204885

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838660_112838661insGA , CM000667.2:g.112838660_112838661insGA	GRCh38
NC_000005.9:g.112174357_112174358insGA , CM000667.1:g.112174357_112174358insGA	GRCh37
NC_000005.8:g.112202256_112202257insGA	NCBI36
NG_008481.4:g.151140_151141insGA , LRG_130:g.151140_151141insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2731_2732insGA	ENSP00000484935.2:n.2731_2732insGA
ENST00000504915.3:c.3120_3121insGA	ENSP00000473355.2:p.Thr1041GlufsTer4
ENST00000505350.2:c.*3072_*3073insGA	ENSP00000481752.1:n.*3072_*3073insGA
ENST00000507379.6:c.3012_3013insGA	ENSP00000423224.2:p.Thr1005GlufsTer4
ENST00000509732.6:c.3066_3067insGA	ENSP00000426541.2:p.Thr1023GlufsTer4
ENST00000512211.7:c.3066_3067insGA	ENSP00000423828.3:p.Thr1023GlufsTer4
ENST00000257430.9:c.3066_3067insGA MANE Select	ENSP00000257430.4:p.Thr1023GlufsTer4
ENST00000257430.8:c.3066_3067insGA	ENSP00000257430.4:p.Thr1023GlufsTer4
ENST00000502371.2:c.1419_1420insGA
ENST00000507379.5:c.3012_3013insGA	ENSP00000423224.1:p.Thr1005GlufsTer4
ENST00000508376.6:c.3066_3067insGA	ENSP00000427089.2:p.Thr1023GlufsTer4
ENST00000508624.5:c.*2388_*2389insGA	ENSP00000424265.1:n.*2388_*2389insGA
ENST00000512211.6:c.3066_3067insGA	ENSP00000423828.2:p.Thr1023GlufsTer4
ENST00000520401.1:c.230+9688_230+9689insGA
NM_000038.5:c.3066_3067insGA	NP_000029.2:p.Thr1023GlufsTer4
NM_001127510.2:c.3066_3067insGA	NP_001120982.1:p.Thr1023GlufsTer4
NM_001127511.2:c.3012_3013insGA	NP_001120983.2:p.Thr1005GlufsTer4
NM_001354895.1:c.3066_3067insGA	NP_001341824.1:p.Thr1023GlufsTer4
NM_001354896.1:c.3120_3121insGA	NP_001341825.1:p.Thr1041GlufsTer4
NM_001354897.1:c.3096_3097insGA	NP_001341826.1:p.Thr1033GlufsTer4
NM_001354898.1:c.2991_2992insGA	NP_001341827.1:p.Thr998GlufsTer4
NM_001354899.1:c.2982_2983insGA	NP_001341828.1:p.Thr995GlufsTer4
NM_001354900.1:c.2943_2944insGA	NP_001341829.1:p.Thr982GlufsTer4
NM_001354901.1:c.2889_2890insGA	NP_001341830.1:p.Thr964GlufsTer4
NM_001354902.1:c.2793_2794insGA	NP_001341831.1:p.Thr932GlufsTer4
NM_001354903.1:c.2763_2764insGA	NP_001341832.1:p.Thr922GlufsTer4
NM_001354904.1:c.2688_2689insGA	NP_001341833.1:p.Thr897GlufsTer4
NM_001354905.1:c.2586_2587insGA	NP_001341834.1:p.Thr863GlufsTer4
NM_001354906.1:c.2217_2218insGA	NP_001341835.1:p.Thr740GlufsTer4
NM_000038.6:c.3066_3067insGA MANE Select	NP_000029.2:p.Thr1023GlufsTer4
NM_001127510.3:c.3066_3067insGA	NP_001120982.1:p.Thr1023GlufsTer4
NM_001127511.3:c.3012_3013insGA	NP_001120983.2:p.Thr1005GlufsTer4
NM_001354895.2:c.3066_3067insGA	NP_001341824.1:p.Thr1023GlufsTer4
NM_001354896.2:c.3120_3121insGA	NP_001341825.1:p.Thr1041GlufsTer4
NM_001354897.2:c.3096_3097insGA	NP_001341826.1:p.Thr1033GlufsTer4
NM_001354898.2:c.2991_2992insGA	NP_001341827.1:p.Thr998GlufsTer4
NM_001354899.2:c.2982_2983insGA	NP_001341828.1:p.Thr995GlufsTer4
NM_001354900.2:c.2943_2944insGA	NP_001341829.1:p.Thr982GlufsTer4
NM_001354901.2:c.2889_2890insGA	NP_001341830.1:p.Thr964GlufsTer4
NM_001354902.2:c.2793_2794insGA	NP_001341831.1:p.Thr932GlufsTer4
NM_001354903.2:c.2763_2764insGA	NP_001341832.1:p.Thr922GlufsTer4
NM_001354904.2:c.2688_2689insGA	NP_001341833.1:p.Thr897GlufsTer4
NM_001354905.2:c.2586_2587insGA	NP_001341834.1:p.Thr863GlufsTer4
NM_001354906.2:c.2217_2218insGA	NP_001341835.1:p.Thr740GlufsTer4