Canonical Allele Identifier: CA2580072774

Gene: APC

Linked Data

• ClinVar Variation Id: 1750226
• ClinVar RCV Id: RCV002353493

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841472_112841474delinsACA , CM000667.2:g.112841472_112841474delinsACA	GRCh38
NC_000005.9:g.112177169_112177171delinsACA , CM000667.1:g.112177169_112177171delinsACA	GRCh37
NC_000005.8:g.112205068_112205070delinsACA	NCBI36
NG_008481.4:g.153952_153954delinsACA , LRG_130:g.153952_153954delinsACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5932_5934delinsACA	ENSP00000473355.2:p.Pro1978Thr
ENST00000505350.2:c.*5884_*5886delinsACA	ENSP00000481752.1:n.*5884_*5886delinsACA
ENST00000507379.6:c.5824_5826delinsACA	ENSP00000423224.2:p.Pro1942Thr
ENST00000509732.6:c.5878_5880delinsACA	ENSP00000426541.2:p.Pro1960Thr
ENST00000512211.7:c.5878_5880delinsACA	ENSP00000423828.3:p.Pro1960Thr
ENST00000257430.9:c.5878_5880delinsACA MANE Select	ENSP00000257430.4:p.Pro1960Thr
ENST00000257430.8:c.5878_5880delinsACA	ENSP00000257430.4:p.Pro1960Thr
ENST00000508376.6:c.5878_5880delinsACA	ENSP00000427089.2:p.Pro1960Thr
ENST00000508624.5:c.*5200_*5202delinsACA	ENSP00000424265.1:n.*5200_*5202delinsACA
ENST00000520401.1:c.230+12500_230+12502delinsACA
NM_000038.5:c.5878_5880delinsACA	NP_000029.2:p.Pro1960Thr
NM_001127510.2:c.5878_5880delinsACA	NP_001120982.1:p.Pro1960Thr
NM_001127511.2:c.5824_5826delinsACA	NP_001120983.2:p.Pro1942Thr
NM_001354895.1:c.5878_5880delinsACA	NP_001341824.1:p.Pro1960Thr
NM_001354896.1:c.5932_5934delinsACA	NP_001341825.1:p.Pro1978Thr
NM_001354897.1:c.5908_5910delinsACA	NP_001341826.1:p.Pro1970Thr
NM_001354898.1:c.5803_5805delinsACA	NP_001341827.1:p.Pro1935Thr
NM_001354899.1:c.5794_5796delinsACA	NP_001341828.1:p.Pro1932Thr
NM_001354900.1:c.5755_5757delinsACA	NP_001341829.1:p.Pro1919Thr
NM_001354901.1:c.5701_5703delinsACA	NP_001341830.1:p.Pro1901Thr
NM_001354902.1:c.5605_5607delinsACA	NP_001341831.1:p.Pro1869Thr
NM_001354903.1:c.5575_5577delinsACA	NP_001341832.1:p.Pro1859Thr
NM_001354904.1:c.5500_5502delinsACA	NP_001341833.1:p.Pro1834Thr
NM_001354905.1:c.5398_5400delinsACA	NP_001341834.1:p.Pro1800Thr
NM_001354906.1:c.5029_5031delinsACA	NP_001341835.1:p.Pro1677Thr
NM_000038.6:c.5878_5880delinsACA MANE Select	NP_000029.2:p.Pro1960Thr
NM_001127510.3:c.5878_5880delinsACA	NP_001120982.1:p.Pro1960Thr
NM_001127511.3:c.5824_5826delinsACA	NP_001120983.2:p.Pro1942Thr
NM_001354895.2:c.5878_5880delinsACA	NP_001341824.1:p.Pro1960Thr
NM_001354896.2:c.5932_5934delinsACA	NP_001341825.1:p.Pro1978Thr
NM_001354897.2:c.5908_5910delinsACA	NP_001341826.1:p.Pro1970Thr
NM_001354898.2:c.5803_5805delinsACA	NP_001341827.1:p.Pro1935Thr
NM_001354899.2:c.5794_5796delinsACA	NP_001341828.1:p.Pro1932Thr
NM_001354900.2:c.5755_5757delinsACA	NP_001341829.1:p.Pro1919Thr
NM_001354901.2:c.5701_5703delinsACA	NP_001341830.1:p.Pro1901Thr
NM_001354902.2:c.5605_5607delinsACA	NP_001341831.1:p.Pro1869Thr
NM_001354903.2:c.5575_5577delinsACA	NP_001341832.1:p.Pro1859Thr
NM_001354904.2:c.5500_5502delinsACA	NP_001341833.1:p.Pro1834Thr
NM_001354905.2:c.5398_5400delinsACA	NP_001341834.1:p.Pro1800Thr
NM_001354906.2:c.5029_5031delinsACA	NP_001341835.1:p.Pro1677Thr