Canonical Allele Identifier: CA1573493034

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819275_112819279delinsGCTTA , CM000667.2:g.112819275_112819279delinsGCTTA	GRCh38
NC_000005.9:g.112154972_112154976delinsGCTTA , CM000667.1:g.112154972_112154976delinsGCTTA	GRCh37
NC_000005.8:g.112182871_112182875delinsGCTTA	NCBI36
NG_008481.4:g.131755_131759delinsGCTTA , LRG_130:g.131755_131759delinsGCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1243_1247delinsGCTTA	ENSP00000484935.2:p.Ala415=
ENST00000504915.3:c.1243_1247delinsGCTTA	ENSP00000473355.2:p.Ala415=
ENST00000505084.2:n.1299_1303delinsGCTTA
ENST00000505350.2:c.*1249_*1253delinsGCTTA	ENSP00000481752.1:n.*1249_*1253delinsGCTTA
ENST00000507379.6:c.1189_1193delinsGCTTA	ENSP00000423224.2:p.Ala397=
ENST00000509732.6:c.1243_1247delinsGCTTA	ENSP00000426541.2:p.Ala415=
ENST00000512211.7:c.1243_1247delinsGCTTA	ENSP00000423828.3:p.Ala415=
ENST00000257430.9:c.1243_1247delinsGCTTA MANE Select	ENSP00000257430.4:p.Ala415=
ENST00000257430.8:c.1243_1247delinsGCTTA	ENSP00000257430.4:p.Ala415=
ENST00000507379.5:c.1189_1193delinsGCTTA	ENSP00000423224.1:p.Ala397=
ENST00000508376.6:c.1243_1247delinsGCTTA	ENSP00000427089.2:p.Ala415=
ENST00000508624.5:c.*565_*569delinsGCTTA	ENSP00000424265.1:n.*565_*569delinsGCTTA
ENST00000512211.6:c.1243_1247delinsGCTTA	ENSP00000423828.2:p.Ala415=
NM_000038.5:c.1243_1247delinsGCTTA	NP_000029.2:p.Ala415=
NM_001127510.2:c.1243_1247delinsGCTTA	NP_001120982.1:p.Ala415=
NM_001127511.2:c.1189_1193delinsGCTTA	NP_001120983.2:p.Ala397=
NM_001354895.1:c.1243_1247delinsGCTTA	NP_001341824.1:p.Ala415=
NM_001354896.1:c.1243_1247delinsGCTTA	NP_001341825.1:p.Ala415=
NM_001354897.1:c.1273_1277delinsGCTTA	NP_001341826.1:p.Ala425=
NM_001354898.1:c.1168_1172delinsGCTTA	NP_001341827.1:p.Ala390=
NM_001354899.1:c.1159_1163delinsGCTTA	NP_001341828.1:p.Ala387=
NM_001354900.1:c.1066_1070delinsGCTTA	NP_001341829.1:p.Ala356=
NM_001354901.1:c.1066_1070delinsGCTTA	NP_001341830.1:p.Ala356=
NM_001354902.1:c.970_974delinsGCTTA	NP_001341831.1:p.Ala324=
NM_001354903.1:c.940_944delinsGCTTA	NP_001341832.1:p.Ala314=
NM_001354904.1:c.865_869delinsGCTTA	NP_001341833.1:p.Ala289=
NM_001354905.1:c.763_767delinsGCTTA	NP_001341834.1:p.Ala255=
NM_001354906.1:c.394_398delinsGCTTA	NP_001341835.1:p.Ala132=
NM_000038.6:c.1243_1247delinsGCTTA MANE Select	NP_000029.2:p.Ala415=
NM_001127510.3:c.1243_1247delinsGCTTA	NP_001120982.1:p.Ala415=
NM_001127511.3:c.1189_1193delinsGCTTA	NP_001120983.2:p.Ala397=
NM_001354895.2:c.1243_1247delinsGCTTA	NP_001341824.1:p.Ala415=
NM_001354896.2:c.1243_1247delinsGCTTA	NP_001341825.1:p.Ala415=
NM_001354897.2:c.1273_1277delinsGCTTA	NP_001341826.1:p.Ala425=
NM_001354898.2:c.1168_1172delinsGCTTA	NP_001341827.1:p.Ala390=
NM_001354899.2:c.1159_1163delinsGCTTA	NP_001341828.1:p.Ala387=
NM_001354900.2:c.1066_1070delinsGCTTA	NP_001341829.1:p.Ala356=
NM_001354901.2:c.1066_1070delinsGCTTA	NP_001341830.1:p.Ala356=
NM_001354902.2:c.970_974delinsGCTTA	NP_001341831.1:p.Ala324=
NM_001354903.2:c.940_944delinsGCTTA	NP_001341832.1:p.Ala314=
NM_001354904.2:c.865_869delinsGCTTA	NP_001341833.1:p.Ala289=
NM_001354905.2:c.763_767delinsGCTTA	NP_001341834.1:p.Ala255=
NM_001354906.2:c.394_398delinsGCTTA	NP_001341835.1:p.Ala132=