Canonical Allele Identifier: CA2695205227

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839517_112839523del , CM000667.2:g.112839517_112839523del	GRCh38
NC_000005.9:g.112175214_112175220del , CM000667.1:g.112175214_112175220del	GRCh37
NC_000005.8:g.112203113_112203119del	NCBI36
NG_008481.4:g.151997_152003del , LRG_130:g.151997_152003del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3588_3594del	ENSP00000484935.2:n.3588_3594del
ENST00000504915.3:c.3977_3983del	ENSP00000473355.2:p.Lys1326ArgfsTer11
ENST00000505350.2:c.*3929_*3935del	ENSP00000481752.1:n.*3929_*3935del
ENST00000507379.6:c.3869_3875del	ENSP00000423224.2:p.Lys1290ArgfsTer11
ENST00000509732.6:c.3923_3929del	ENSP00000426541.2:p.Lys1308ArgfsTer11
ENST00000512211.7:c.3923_3929del	ENSP00000423828.3:p.Lys1308ArgfsTer11
ENST00000257430.9:c.3923_3929del MANE Select	ENSP00000257430.4:p.Lys1308ArgfsTer11
ENST00000257430.8:c.3923_3929del	ENSP00000257430.4:p.Lys1308ArgfsTer11
ENST00000502371.2:c.2276_2282del
ENST00000508376.6:c.3923_3929del	ENSP00000427089.2:p.Lys1308ArgfsTer11
ENST00000508624.5:c.*3245_*3251del	ENSP00000424265.1:n.*3245_*3251del
ENST00000520401.1:c.230+10545_230+10551del
NM_000038.5:c.3923_3929del	NP_000029.2:p.Lys1308ArgfsTer11
NM_001127510.2:c.3923_3929del	NP_001120982.1:p.Lys1308ArgfsTer11
NM_001127511.2:c.3869_3875del	NP_001120983.2:p.Lys1290ArgfsTer11
NM_001354895.1:c.3923_3929del	NP_001341824.1:p.Lys1308ArgfsTer11
NM_001354896.1:c.3977_3983del	NP_001341825.1:p.Lys1326ArgfsTer11
NM_001354897.1:c.3953_3959del	NP_001341826.1:p.Lys1318ArgfsTer11
NM_001354898.1:c.3848_3854del	NP_001341827.1:p.Lys1283ArgfsTer11
NM_001354899.1:c.3839_3845del	NP_001341828.1:p.Lys1280ArgfsTer11
NM_001354900.1:c.3800_3806del	NP_001341829.1:p.Lys1267ArgfsTer11
NM_001354901.1:c.3746_3752del	NP_001341830.1:p.Lys1249ArgfsTer11
NM_001354902.1:c.3650_3656del	NP_001341831.1:p.Lys1217ArgfsTer11
NM_001354903.1:c.3620_3626del	NP_001341832.1:p.Lys1207ArgfsTer11
NM_001354904.1:c.3545_3551del	NP_001341833.1:p.Lys1182ArgfsTer11
NM_001354905.1:c.3443_3449del	NP_001341834.1:p.Lys1148ArgfsTer11
NM_001354906.1:c.3074_3080del	NP_001341835.1:p.Lys1025ArgfsTer11
NM_000038.6:c.3923_3929del MANE Select	NP_000029.2:p.Lys1308ArgfsTer11
NM_001127510.3:c.3923_3929del	NP_001120982.1:p.Lys1308ArgfsTer11
NM_001127511.3:c.3869_3875del	NP_001120983.2:p.Lys1290ArgfsTer11
NM_001354895.2:c.3923_3929del	NP_001341824.1:p.Lys1308ArgfsTer11
NM_001354896.2:c.3977_3983del	NP_001341825.1:p.Lys1326ArgfsTer11
NM_001354897.2:c.3953_3959del	NP_001341826.1:p.Lys1318ArgfsTer11
NM_001354898.2:c.3848_3854del	NP_001341827.1:p.Lys1283ArgfsTer11
NM_001354899.2:c.3839_3845del	NP_001341828.1:p.Lys1280ArgfsTer11
NM_001354900.2:c.3800_3806del	NP_001341829.1:p.Lys1267ArgfsTer11
NM_001354901.2:c.3746_3752del	NP_001341830.1:p.Lys1249ArgfsTer11
NM_001354902.2:c.3650_3656del	NP_001341831.1:p.Lys1217ArgfsTer11
NM_001354903.2:c.3620_3626del	NP_001341832.1:p.Lys1207ArgfsTer11
NM_001354904.2:c.3545_3551del	NP_001341833.1:p.Lys1182ArgfsTer11
NM_001354905.2:c.3443_3449del	NP_001341834.1:p.Lys1148ArgfsTer11
NM_001354906.2:c.3074_3080del	NP_001341835.1:p.Lys1025ArgfsTer11