Canonical Allele Identifier: CA2695204929

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838953dup , CM000667.2:g.112838953dup	GRCh38
NC_000005.9:g.112174650dup , CM000667.1:g.112174650dup	GRCh37
NC_000005.8:g.112202549dup	NCBI36
NG_008481.4:g.151433dup , LRG_130:g.151433dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3024dup	ENSP00000484935.2:n.3024dup
ENST00000504915.3:c.3413dup	ENSP00000473355.2:p.Ile1139AsnfsTer2
ENST00000505350.2:c.*3365dup	ENSP00000481752.1:n.*3365dup
ENST00000507379.6:c.3305dup	ENSP00000423224.2:p.Ile1103AsnfsTer2
ENST00000509732.6:c.3359dup	ENSP00000426541.2:p.Ile1121AsnfsTer2
ENST00000512211.7:c.3359dup	ENSP00000423828.3:p.Ile1121AsnfsTer2
ENST00000257430.9:c.3359dup MANE Select	ENSP00000257430.4:p.Ile1121AsnfsTer2
ENST00000257430.8:c.3359dup	ENSP00000257430.4:p.Ile1121AsnfsTer2
ENST00000502371.2:c.1712dup
ENST00000507379.5:c.3305dup	ENSP00000423224.1:p.Ile1103AsnfsTer2
ENST00000508376.6:c.3359dup	ENSP00000427089.2:p.Ile1121AsnfsTer2
ENST00000508624.5:c.*2681dup	ENSP00000424265.1:n.*2681dup
ENST00000512211.6:c.3359dup	ENSP00000423828.2:p.Ile1121AsnfsTer2
ENST00000520401.1:c.230+9981dup
NM_000038.5:c.3359dup	NP_000029.2:p.Ile1121AsnfsTer2
NM_001127510.2:c.3359dup	NP_001120982.1:p.Ile1121AsnfsTer2
NM_001127511.2:c.3305dup	NP_001120983.2:p.Ile1103AsnfsTer2
NM_001354895.1:c.3359dup	NP_001341824.1:p.Ile1121AsnfsTer2
NM_001354896.1:c.3413dup	NP_001341825.1:p.Ile1139AsnfsTer2
NM_001354897.1:c.3389dup	NP_001341826.1:p.Ile1131AsnfsTer2
NM_001354898.1:c.3284dup	NP_001341827.1:p.Ile1096AsnfsTer2
NM_001354899.1:c.3275dup	NP_001341828.1:p.Ile1093AsnfsTer2
NM_001354900.1:c.3236dup	NP_001341829.1:p.Ile1080AsnfsTer2
NM_001354901.1:c.3182dup	NP_001341830.1:p.Ile1062AsnfsTer2
NM_001354902.1:c.3086dup	NP_001341831.1:p.Ile1030AsnfsTer2
NM_001354903.1:c.3056dup	NP_001341832.1:p.Ile1020AsnfsTer2
NM_001354904.1:c.2981dup	NP_001341833.1:p.Ile995AsnfsTer2
NM_001354905.1:c.2879dup	NP_001341834.1:p.Ile961AsnfsTer2
NM_001354906.1:c.2510dup	NP_001341835.1:p.Ile838AsnfsTer2
NM_000038.6:c.3359dup MANE Select	NP_000029.2:p.Ile1121AsnfsTer2
NM_001127510.3:c.3359dup	NP_001120982.1:p.Ile1121AsnfsTer2
NM_001127511.3:c.3305dup	NP_001120983.2:p.Ile1103AsnfsTer2
NM_001354895.2:c.3359dup	NP_001341824.1:p.Ile1121AsnfsTer2
NM_001354896.2:c.3413dup	NP_001341825.1:p.Ile1139AsnfsTer2
NM_001354897.2:c.3389dup	NP_001341826.1:p.Ile1131AsnfsTer2
NM_001354898.2:c.3284dup	NP_001341827.1:p.Ile1096AsnfsTer2
NM_001354899.2:c.3275dup	NP_001341828.1:p.Ile1093AsnfsTer2
NM_001354900.2:c.3236dup	NP_001341829.1:p.Ile1080AsnfsTer2
NM_001354901.2:c.3182dup	NP_001341830.1:p.Ile1062AsnfsTer2
NM_001354902.2:c.3086dup	NP_001341831.1:p.Ile1030AsnfsTer2
NM_001354903.2:c.3056dup	NP_001341832.1:p.Ile1020AsnfsTer2
NM_001354904.2:c.2981dup	NP_001341833.1:p.Ile995AsnfsTer2
NM_001354905.2:c.2879dup	NP_001341834.1:p.Ile961AsnfsTer2
NM_001354906.2:c.2510dup	NP_001341835.1:p.Ile838AsnfsTer2