Canonical Allele Identifier: CA2695202726

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821915dup , CM000667.2:g.112821915dup	GRCh38
NC_000005.9:g.112157612dup , CM000667.1:g.112157612dup	GRCh37
NC_000005.8:g.112185511dup	NCBI36
NG_008481.4:g.134395dup , LRG_130:g.134395dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1332dup	ENSP00000484935.2:p.Gln445SerfsTer15
ENST00000504915.3:c.1332dup	ENSP00000473355.2:p.Gln445SerfsTer15
ENST00000505084.2:n.1388dup
ENST00000505350.2:c.*1338dup	ENSP00000481752.1:n.*1338dup
ENST00000507379.6:c.1278dup	ENSP00000423224.2:p.Gln427SerfsTer15
ENST00000509732.6:c.1332dup	ENSP00000426541.2:p.Gln445SerfsTer15
ENST00000512211.7:c.1332dup	ENSP00000423828.3:p.Gln445SerfsTer15
ENST00000257430.9:c.1332dup MANE Select	ENSP00000257430.4:p.Gln445SerfsTer15
ENST00000257430.8:c.1332dup	ENSP00000257430.4:p.Gln445SerfsTer15
ENST00000502371.2:c.20dup
ENST00000507379.5:c.1278dup	ENSP00000423224.1:p.Gln427SerfsTer15
ENST00000508376.6:c.1332dup	ENSP00000427089.2:p.Gln445SerfsTer15
ENST00000508624.5:c.*654dup	ENSP00000424265.1:n.*654dup
ENST00000512211.6:c.1332dup	ENSP00000423828.2:p.Gln445SerfsTer15
NM_000038.5:c.1332dup	NP_000029.2:p.Gln445SerfsTer15
NM_001127510.2:c.1332dup	NP_001120982.1:p.Gln445SerfsTer15
NM_001127511.2:c.1278dup	NP_001120983.2:p.Gln427SerfsTer15
NM_001354895.1:c.1332dup	NP_001341824.1:p.Gln445SerfsTer15
NM_001354896.1:c.1332dup	NP_001341825.1:p.Gln445SerfsTer15
NM_001354897.1:c.1362dup	NP_001341826.1:p.Gln455SerfsTer15
NM_001354898.1:c.1257dup	NP_001341827.1:p.Gln420SerfsTer15
NM_001354899.1:c.1248dup	NP_001341828.1:p.Gln417SerfsTer15
NM_001354900.1:c.1155dup	NP_001341829.1:p.Gln386SerfsTer15
NM_001354901.1:c.1155dup	NP_001341830.1:p.Gln386SerfsTer15
NM_001354902.1:c.1059dup	NP_001341831.1:p.Gln354SerfsTer15
NM_001354903.1:c.1029dup	NP_001341832.1:p.Gln344SerfsTer15
NM_001354904.1:c.954dup	NP_001341833.1:p.Gln319SerfsTer15
NM_001354905.1:c.852dup	NP_001341834.1:p.Gln285SerfsTer15
NM_001354906.1:c.483dup	NP_001341835.1:p.Gln162SerfsTer15
NM_000038.6:c.1332dup MANE Select	NP_000029.2:p.Gln445SerfsTer15
NM_001127510.3:c.1332dup	NP_001120982.1:p.Gln445SerfsTer15
NM_001127511.3:c.1278dup	NP_001120983.2:p.Gln427SerfsTer15
NM_001354895.2:c.1332dup	NP_001341824.1:p.Gln445SerfsTer15
NM_001354896.2:c.1332dup	NP_001341825.1:p.Gln445SerfsTer15
NM_001354897.2:c.1362dup	NP_001341826.1:p.Gln455SerfsTer15
NM_001354898.2:c.1257dup	NP_001341827.1:p.Gln420SerfsTer15
NM_001354899.2:c.1248dup	NP_001341828.1:p.Gln417SerfsTer15
NM_001354900.2:c.1155dup	NP_001341829.1:p.Gln386SerfsTer15
NM_001354901.2:c.1155dup	NP_001341830.1:p.Gln386SerfsTer15
NM_001354902.2:c.1059dup	NP_001341831.1:p.Gln354SerfsTer15
NM_001354903.2:c.1029dup	NP_001341832.1:p.Gln344SerfsTer15
NM_001354904.2:c.954dup	NP_001341833.1:p.Gln319SerfsTer15
NM_001354905.2:c.852dup	NP_001341834.1:p.Gln285SerfsTer15
NM_001354906.2:c.483dup	NP_001341835.1:p.Gln162SerfsTer15