Canonical Allele Identifier: CA2695204919

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838879_112838880delinsAT , CM000667.2:g.112838879_112838880delinsAT	GRCh38
NC_000005.9:g.112174576_112174577delinsAT , CM000667.1:g.112174576_112174577delinsAT	GRCh37
NC_000005.8:g.112202475_112202476delinsAT	NCBI36
NG_008481.4:g.151359_151360delinsAT , LRG_130:g.151359_151360delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2950_2951delinsAT	ENSP00000484935.2:n.2950_2951delinsAT
ENST00000504915.3:c.3339_3340delinsAT	ENSP00000473355.2:p.Gln1114Ter
ENST00000505350.2:c.*3291_*3292delinsAT	ENSP00000481752.1:n.*3291_*3292delinsAT
ENST00000507379.6:c.3231_3232delinsAT	ENSP00000423224.2:p.Gln1078Ter
ENST00000509732.6:c.3285_3286delinsAT	ENSP00000426541.2:p.Gln1096Ter
ENST00000512211.7:c.3285_3286delinsAT	ENSP00000423828.3:p.Gln1096Ter
ENST00000257430.9:c.3285_3286delinsAT MANE Select	ENSP00000257430.4:p.Gln1096Ter
ENST00000257430.8:c.3285_3286delinsAT	ENSP00000257430.4:p.Gln1096Ter
ENST00000502371.2:c.1638_1639delinsAT
ENST00000507379.5:c.3231_3232delinsAT	ENSP00000423224.1:p.Gln1078Ter
ENST00000508376.6:c.3285_3286delinsAT	ENSP00000427089.2:p.Gln1096Ter
ENST00000508624.5:c.*2607_*2608delinsAT	ENSP00000424265.1:n.*2607_*2608delinsAT
ENST00000512211.6:c.3285_3286delinsAT	ENSP00000423828.2:p.Gln1096Ter
ENST00000520401.1:c.230+9907_230+9908delinsAT
NM_000038.5:c.3285_3286delinsAT	NP_000029.2:p.Gln1096Ter
NM_001127510.2:c.3285_3286delinsAT	NP_001120982.1:p.Gln1096Ter
NM_001127511.2:c.3231_3232delinsAT	NP_001120983.2:p.Gln1078Ter
NM_001354895.1:c.3285_3286delinsAT	NP_001341824.1:p.Gln1096Ter
NM_001354896.1:c.3339_3340delinsAT	NP_001341825.1:p.Gln1114Ter
NM_001354897.1:c.3315_3316delinsAT	NP_001341826.1:p.Gln1106Ter
NM_001354898.1:c.3210_3211delinsAT	NP_001341827.1:p.Gln1071Ter
NM_001354899.1:c.3201_3202delinsAT	NP_001341828.1:p.Gln1068Ter
NM_001354900.1:c.3162_3163delinsAT	NP_001341829.1:p.Gln1055Ter
NM_001354901.1:c.3108_3109delinsAT	NP_001341830.1:p.Gln1037Ter
NM_001354902.1:c.3012_3013delinsAT	NP_001341831.1:p.Gln1005Ter
NM_001354903.1:c.2982_2983delinsAT	NP_001341832.1:p.Gln995Ter
NM_001354904.1:c.2907_2908delinsAT	NP_001341833.1:p.Gln970Ter
NM_001354905.1:c.2805_2806delinsAT	NP_001341834.1:p.Gln936Ter
NM_001354906.1:c.2436_2437delinsAT	NP_001341835.1:p.Gln813Ter
NM_000038.6:c.3285_3286delinsAT MANE Select	NP_000029.2:p.Gln1096Ter
NM_001127510.3:c.3285_3286delinsAT	NP_001120982.1:p.Gln1096Ter
NM_001127511.3:c.3231_3232delinsAT	NP_001120983.2:p.Gln1078Ter
NM_001354895.2:c.3285_3286delinsAT	NP_001341824.1:p.Gln1096Ter
NM_001354896.2:c.3339_3340delinsAT	NP_001341825.1:p.Gln1114Ter
NM_001354897.2:c.3315_3316delinsAT	NP_001341826.1:p.Gln1106Ter
NM_001354898.2:c.3210_3211delinsAT	NP_001341827.1:p.Gln1071Ter
NM_001354899.2:c.3201_3202delinsAT	NP_001341828.1:p.Gln1068Ter
NM_001354900.2:c.3162_3163delinsAT	NP_001341829.1:p.Gln1055Ter
NM_001354901.2:c.3108_3109delinsAT	NP_001341830.1:p.Gln1037Ter
NM_001354902.2:c.3012_3013delinsAT	NP_001341831.1:p.Gln1005Ter
NM_001354903.2:c.2982_2983delinsAT	NP_001341832.1:p.Gln995Ter
NM_001354904.2:c.2907_2908delinsAT	NP_001341833.1:p.Gln970Ter
NM_001354905.2:c.2805_2806delinsAT	NP_001341834.1:p.Gln936Ter
NM_001354906.2:c.2436_2437delinsAT	NP_001341835.1:p.Gln813Ter