Canonical Allele Identifier: CA2695204959

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839324_112839327del , CM000667.2:g.112839324_112839327del	GRCh38
NC_000005.9:g.112175021_112175024del , CM000667.1:g.112175021_112175024del	GRCh37
NC_000005.8:g.112202920_112202923del	NCBI36
NG_008481.4:g.151804_151807del , LRG_130:g.151804_151807del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3395_3398del	ENSP00000484935.2:n.3395_3398del
ENST00000504915.3:c.3784_3787del	ENSP00000473355.2:p.Gln1262ArgfsTer20
ENST00000505350.2:c.*3736_*3739del	ENSP00000481752.1:n.*3736_*3739del
ENST00000507379.6:c.3676_3679del	ENSP00000423224.2:p.Gln1226ArgfsTer20
ENST00000509732.6:c.3730_3733del	ENSP00000426541.2:p.Gln1244ArgfsTer20
ENST00000512211.7:c.3730_3733del	ENSP00000423828.3:p.Gln1244ArgfsTer20
ENST00000257430.9:c.3730_3733del MANE Select	ENSP00000257430.4:p.Gln1244ArgfsTer20
ENST00000257430.8:c.3730_3733del	ENSP00000257430.4:p.Gln1244ArgfsTer20
ENST00000502371.2:c.2083_2086del
ENST00000508376.6:c.3730_3733del	ENSP00000427089.2:p.Gln1244ArgfsTer20
ENST00000508624.5:c.*3052_*3055del	ENSP00000424265.1:n.*3052_*3055del
ENST00000512211.6:c.3730_3733del	ENSP00000423828.2:p.Gln1244ArgfsTer20
ENST00000520401.1:c.230+10352_230+10355del
NM_000038.5:c.3730_3733del	NP_000029.2:p.Gln1244ArgfsTer20
NM_001127510.2:c.3730_3733del	NP_001120982.1:p.Gln1244ArgfsTer20
NM_001127511.2:c.3676_3679del	NP_001120983.2:p.Gln1226ArgfsTer20
NM_001354895.1:c.3730_3733del	NP_001341824.1:p.Gln1244ArgfsTer20
NM_001354896.1:c.3784_3787del	NP_001341825.1:p.Gln1262ArgfsTer20
NM_001354897.1:c.3760_3763del	NP_001341826.1:p.Gln1254ArgfsTer20
NM_001354898.1:c.3655_3658del	NP_001341827.1:p.Gln1219ArgfsTer20
NM_001354899.1:c.3646_3649del	NP_001341828.1:p.Gln1216ArgfsTer20
NM_001354900.1:c.3607_3610del	NP_001341829.1:p.Gln1203ArgfsTer20
NM_001354901.1:c.3553_3556del	NP_001341830.1:p.Gln1185ArgfsTer20
NM_001354902.1:c.3457_3460del	NP_001341831.1:p.Gln1153ArgfsTer20
NM_001354903.1:c.3427_3430del	NP_001341832.1:p.Gln1143ArgfsTer20
NM_001354904.1:c.3352_3355del	NP_001341833.1:p.Gln1118ArgfsTer20
NM_001354905.1:c.3250_3253del	NP_001341834.1:p.Gln1084ArgfsTer20
NM_001354906.1:c.2881_2884del	NP_001341835.1:p.Gln961ArgfsTer20
NM_000038.6:c.3730_3733del MANE Select	NP_000029.2:p.Gln1244ArgfsTer20
NM_001127510.3:c.3730_3733del	NP_001120982.1:p.Gln1244ArgfsTer20
NM_001127511.3:c.3676_3679del	NP_001120983.2:p.Gln1226ArgfsTer20
NM_001354895.2:c.3730_3733del	NP_001341824.1:p.Gln1244ArgfsTer20
NM_001354896.2:c.3784_3787del	NP_001341825.1:p.Gln1262ArgfsTer20
NM_001354897.2:c.3760_3763del	NP_001341826.1:p.Gln1254ArgfsTer20
NM_001354898.2:c.3655_3658del	NP_001341827.1:p.Gln1219ArgfsTer20
NM_001354899.2:c.3646_3649del	NP_001341828.1:p.Gln1216ArgfsTer20
NM_001354900.2:c.3607_3610del	NP_001341829.1:p.Gln1203ArgfsTer20
NM_001354901.2:c.3553_3556del	NP_001341830.1:p.Gln1185ArgfsTer20
NM_001354902.2:c.3457_3460del	NP_001341831.1:p.Gln1153ArgfsTer20
NM_001354903.2:c.3427_3430del	NP_001341832.1:p.Gln1143ArgfsTer20
NM_001354904.2:c.3352_3355del	NP_001341833.1:p.Gln1118ArgfsTer20
NM_001354905.2:c.3250_3253del	NP_001341834.1:p.Gln1084ArgfsTer20
NM_001354906.2:c.2881_2884del	NP_001341835.1:p.Gln961ArgfsTer20