Canonical Allele Identifier: CA1573487658

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112785860_112785863delinsATCT , CM000667.2:g.112785860_112785863delinsATCT	GRCh38
NC_000005.9:g.112121557_112121560delinsATCT , CM000667.1:g.112121557_112121560delinsATCT	GRCh37
NC_000005.8:g.112149456_112149459delinsATCT	NCBI36
NG_008481.4:g.98340_98343delinsATCT , LRG_130:g.98340_98343delinsATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.645+4957_645+4960delinsATCT	ENSP00000484935.2:n.645+4957_645+4960delinsATCT
ENST00000504915.3:c.645+4957_645+4960delinsATCT	ENSP00000473355.2:n.645+4957_645+4960delinsATCT
ENST00000505084.2:n.701+4957_701+4960delinsATCT
ENST00000505350.2:c.*651+4957_*651+4960delinsATCT	ENSP00000481752.1:n.*651+4957_*651+4960delinsATCT
ENST00000507379.6:c.675+4957_675+4960delinsATCT	ENSP00000423224.2:n.675+4957_675+4960delinsATCT
ENST00000509732.6:c.645+4957_645+4960delinsATCT	ENSP00000426541.2:n.645+4957_645+4960delinsATCT
ENST00000512211.7:c.645+4957_645+4960delinsATCT	ENSP00000423828.3:n.645+4957_645+4960delinsATCT
ENST00000257430.9:c.645+4957_645+4960delinsATCT MANE Select	ENSP00000257430.4:n.645+4957_645+4960delinsATCT
ENST00000257430.8:c.645+4957_645+4960delinsATCT	ENSP00000257430.4:n.645+4957_645+4960delinsATCT
ENST00000507379.5:c.675+4957_675+4960delinsATCT	ENSP00000423224.1:n.675+4957_675+4960delinsATCT
ENST00000508376.6:c.645+4957_645+4960delinsATCT	ENSP00000427089.2:n.645+4957_645+4960delinsATCT
ENST00000508624.5:c.645+4957_645+4960delinsATCT	ENSP00000424265.1:n.645+4957_645+4960delinsATCT
ENST00000512211.6:c.645+4957_645+4960delinsATCT	ENSP00000423828.2:n.645+4957_645+4960delinsATCT
NM_000038.5:c.645+4957_645+4960delinsATCT	NP_000029.2:n.645+4957_645+4960delinsATCT
NM_001127510.2:c.645+4957_645+4960delinsATCT	NP_001120982.1:n.645+4957_645+4960delinsATCT
NM_001127511.2:c.675+4957_675+4960delinsATCT	NP_001120983.2:n.675+4957_675+4960delinsATCT
NM_001354895.1:c.645+4957_645+4960delinsATCT	NP_001341824.1:n.645+4957_645+4960delinsATCT
NM_001354896.1:c.645+4957_645+4960delinsATCT	NP_001341825.1:n.645+4957_645+4960delinsATCT
NM_001354897.1:c.675+4957_675+4960delinsATCT	NP_001341826.1:n.675+4957_675+4960delinsATCT
NM_001354898.1:c.570+4957_570+4960delinsATCT	NP_001341827.1:n.570+4957_570+4960delinsATCT
NM_001354899.1:c.645+4957_645+4960delinsATCT	NP_001341828.1:n.645+4957_645+4960delinsATCT
NM_001354900.1:c.468+4957_468+4960delinsATCT	NP_001341829.1:n.468+4957_468+4960delinsATCT
NM_001354901.1:c.468+4957_468+4960delinsATCT	NP_001341830.1:n.468+4957_468+4960delinsATCT
NM_001354902.1:c.675+4957_675+4960delinsATCT	NP_001341831.1:n.675+4957_675+4960delinsATCT
NM_001354903.1:c.645+4957_645+4960delinsATCT	NP_001341832.1:n.645+4957_645+4960delinsATCT
NM_001354904.1:c.570+4957_570+4960delinsATCT	NP_001341833.1:n.570+4957_570+4960delinsATCT
NM_001354905.1:c.468+4957_468+4960delinsATCT	NP_001341834.1:n.468+4957_468+4960delinsATCT
NM_001354906.1:c.-391+4957_-391+4960delinsATCT	NP_001341835.1:n.-391+4957_-391+4960delinsATCT
NM_000038.6:c.645+4957_645+4960delinsATCT MANE Select	NP_000029.2:n.645+4957_645+4960delinsATCT
NM_001127510.3:c.645+4957_645+4960delinsATCT	NP_001120982.1:n.645+4957_645+4960delinsATCT
NM_001127511.3:c.675+4957_675+4960delinsATCT	NP_001120983.2:n.675+4957_675+4960delinsATCT
NM_001354895.2:c.645+4957_645+4960delinsATCT	NP_001341824.1:n.645+4957_645+4960delinsATCT
NM_001354896.2:c.645+4957_645+4960delinsATCT	NP_001341825.1:n.645+4957_645+4960delinsATCT
NM_001354897.2:c.675+4957_675+4960delinsATCT	NP_001341826.1:n.675+4957_675+4960delinsATCT
NM_001354898.2:c.570+4957_570+4960delinsATCT	NP_001341827.1:n.570+4957_570+4960delinsATCT
NM_001354899.2:c.645+4957_645+4960delinsATCT	NP_001341828.1:n.645+4957_645+4960delinsATCT
NM_001354900.2:c.468+4957_468+4960delinsATCT	NP_001341829.1:n.468+4957_468+4960delinsATCT
NM_001354901.2:c.468+4957_468+4960delinsATCT	NP_001341830.1:n.468+4957_468+4960delinsATCT
NM_001354902.2:c.675+4957_675+4960delinsATCT	NP_001341831.1:n.675+4957_675+4960delinsATCT
NM_001354903.2:c.645+4957_645+4960delinsATCT	NP_001341832.1:n.645+4957_645+4960delinsATCT
NM_001354904.2:c.570+4957_570+4960delinsATCT	NP_001341833.1:n.570+4957_570+4960delinsATCT
NM_001354905.2:c.468+4957_468+4960delinsATCT	NP_001341834.1:n.468+4957_468+4960delinsATCT
NM_001354906.2:c.-391+4957_-391+4960delinsATCT	NP_001341835.1:n.-391+4957_-391+4960delinsATCT