Canonical Allele Identifier: CA1573485575

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838628_112838631delinsAATC , CM000667.2:g.112838628_112838631delinsAATC	GRCh38
NC_000005.9:g.112174325_112174328delinsAATC , CM000667.1:g.112174325_112174328delinsAATC	GRCh37
NC_000005.8:g.112202224_112202227delinsAATC	NCBI36
NG_008481.4:g.151108_151111delinsAATC , LRG_130:g.151108_151111delinsAATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2699_2702delinsAATC	ENSP00000484935.2:n.2699_2702delinsAATC
ENST00000504915.3:c.3088_3091delinsAATC	ENSP00000473355.2:p.Asn1030=
ENST00000505350.2:c.*3040_*3043delinsAATC	ENSP00000481752.1:n.*3040_*3043delinsAATC
ENST00000507379.6:c.2980_2983delinsAATC	ENSP00000423224.2:p.Asn994=
ENST00000509732.6:c.3034_3037delinsAATC	ENSP00000426541.2:p.Asn1012=
ENST00000512211.7:c.3034_3037delinsAATC	ENSP00000423828.3:p.Asn1012=
ENST00000257430.9:c.3034_3037delinsAATC MANE Select	ENSP00000257430.4:p.Asn1012=
ENST00000257430.8:c.3034_3037delinsAATC	ENSP00000257430.4:p.Asn1012=
ENST00000502371.2:c.1387_1390delinsAATC
ENST00000507379.5:c.2980_2983delinsAATC	ENSP00000423224.1:p.Asn994=
ENST00000508376.6:c.3034_3037delinsAATC	ENSP00000427089.2:p.Asn1012=
ENST00000508624.5:c.*2356_*2359delinsAATC	ENSP00000424265.1:n.*2356_*2359delinsAATC
ENST00000512211.6:c.3034_3037delinsAATC	ENSP00000423828.2:p.Asn1012=
ENST00000520401.1:c.230+9656_230+9659delinsAATC
NM_000038.5:c.3034_3037delinsAATC	NP_000029.2:p.Asn1012=
NM_001127510.2:c.3034_3037delinsAATC	NP_001120982.1:p.Asn1012=
NM_001127511.2:c.2980_2983delinsAATC	NP_001120983.2:p.Asn994=
NM_001354895.1:c.3034_3037delinsAATC	NP_001341824.1:p.Asn1012=
NM_001354896.1:c.3088_3091delinsAATC	NP_001341825.1:p.Asn1030=
NM_001354897.1:c.3064_3067delinsAATC	NP_001341826.1:p.Asn1022=
NM_001354898.1:c.2959_2962delinsAATC	NP_001341827.1:p.Asn987=
NM_001354899.1:c.2950_2953delinsAATC	NP_001341828.1:p.Asn984=
NM_001354900.1:c.2911_2914delinsAATC	NP_001341829.1:p.Asn971=
NM_001354901.1:c.2857_2860delinsAATC	NP_001341830.1:p.Asn953=
NM_001354902.1:c.2761_2764delinsAATC	NP_001341831.1:p.Asn921=
NM_001354903.1:c.2731_2734delinsAATC	NP_001341832.1:p.Asn911=
NM_001354904.1:c.2656_2659delinsAATC	NP_001341833.1:p.Asn886=
NM_001354905.1:c.2554_2557delinsAATC	NP_001341834.1:p.Asn852=
NM_001354906.1:c.2185_2188delinsAATC	NP_001341835.1:p.Asn729=
NM_000038.6:c.3034_3037delinsAATC MANE Select	NP_000029.2:p.Asn1012=
NM_001127510.3:c.3034_3037delinsAATC	NP_001120982.1:p.Asn1012=
NM_001127511.3:c.2980_2983delinsAATC	NP_001120983.2:p.Asn994=
NM_001354895.2:c.3034_3037delinsAATC	NP_001341824.1:p.Asn1012=
NM_001354896.2:c.3088_3091delinsAATC	NP_001341825.1:p.Asn1030=
NM_001354897.2:c.3064_3067delinsAATC	NP_001341826.1:p.Asn1022=
NM_001354898.2:c.2959_2962delinsAATC	NP_001341827.1:p.Asn987=
NM_001354899.2:c.2950_2953delinsAATC	NP_001341828.1:p.Asn984=
NM_001354900.2:c.2911_2914delinsAATC	NP_001341829.1:p.Asn971=
NM_001354901.2:c.2857_2860delinsAATC	NP_001341830.1:p.Asn953=
NM_001354902.2:c.2761_2764delinsAATC	NP_001341831.1:p.Asn921=
NM_001354903.2:c.2731_2734delinsAATC	NP_001341832.1:p.Asn911=
NM_001354904.2:c.2656_2659delinsAATC	NP_001341833.1:p.Asn886=
NM_001354905.2:c.2554_2557delinsAATC	NP_001341834.1:p.Asn852=
NM_001354906.2:c.2185_2188delinsAATC	NP_001341835.1:p.Asn729=