Canonical Allele Identifier: CA445758926

Gene: APC

Linked Data

• COSMIC: COSM19656
• MyVariant Identifiers: chr5:g.112170824del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835127del , CM000667.2:g.112835127del	GRCh38
NC_000005.9:g.112170824del , CM000667.1:g.112170824del	GRCh37
NC_000005.8:g.112198723del	NCBI36
NG_008481.4:g.147607del , LRG_130:g.147607del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1585del	ENSP00000484935.2:n.1585del
ENST00000504915.3:c.1974del	ENSP00000473355.2:p.Asn659MetfsTer5
ENST00000505350.2:c.*1926del	ENSP00000481752.1:n.*1926del
ENST00000507379.6:c.1866del	ENSP00000423224.2:p.Asn623MetfsTer5
ENST00000509732.6:c.1920del	ENSP00000426541.2:p.Asn641MetfsTer5
ENST00000512211.7:c.1920del	ENSP00000423828.3:p.Asn641MetfsTer5
ENST00000257430.9:c.1920del MANE Select	ENSP00000257430.4:p.Asn641MetfsTer5
ENST00000257430.8:c.1920del	ENSP00000257430.4:p.Asn641MetfsTer5
ENST00000502371.2:c.273del
ENST00000504915.2:c.609del	ENSP00000473355.1:p.Asn204MetfsTer5
ENST00000507379.5:c.1866del	ENSP00000423224.1:p.Asn623MetfsTer5
ENST00000508376.6:c.1920del	ENSP00000427089.2:p.Asn641MetfsTer5
ENST00000508624.5:c.*1242del	ENSP00000424265.1:n.*1242del
ENST00000512211.6:c.1920del	ENSP00000423828.2:p.Asn641MetfsTer5
ENST00000520401.1:c.230+6155del
NM_000038.5:c.1920del	NP_000029.2:p.Asn641MetfsTer5
NM_001127510.2:c.1920del	NP_001120982.1:p.Asn641MetfsTer5
NM_001127511.2:c.1866del	NP_001120983.2:p.Asn623MetfsTer5
NM_001354895.1:c.1920del	NP_001341824.1:p.Asn641MetfsTer5
NM_001354896.1:c.1974del	NP_001341825.1:p.Asn659MetfsTer5
NM_001354897.1:c.1950del	NP_001341826.1:p.Asn651MetfsTer5
NM_001354898.1:c.1845del	NP_001341827.1:p.Asn616MetfsTer5
NM_001354899.1:c.1836del	NP_001341828.1:p.Asn613MetfsTer5
NM_001354900.1:c.1797del	NP_001341829.1:p.Asn600MetfsTer5
NM_001354901.1:c.1743del	NP_001341830.1:p.Asn582MetfsTer5
NM_001354902.1:c.1647del	NP_001341831.1:p.Asn550MetfsTer5
NM_001354903.1:c.1617del	NP_001341832.1:p.Asn540MetfsTer5
NM_001354904.1:c.1542del	NP_001341833.1:p.Asn515MetfsTer5
NM_001354905.1:c.1440del	NP_001341834.1:p.Asn481MetfsTer5
NM_001354906.1:c.1071del	NP_001341835.1:p.Asn358MetfsTer5
NM_000038.6:c.1920del MANE Select	NP_000029.2:p.Asn641MetfsTer5
NM_001127510.3:c.1920del	NP_001120982.1:p.Asn641MetfsTer5
NM_001127511.3:c.1866del	NP_001120983.2:p.Asn623MetfsTer5
NM_001354895.2:c.1920del	NP_001341824.1:p.Asn641MetfsTer5
NM_001354896.2:c.1974del	NP_001341825.1:p.Asn659MetfsTer5
NM_001354897.2:c.1950del	NP_001341826.1:p.Asn651MetfsTer5
NM_001354898.2:c.1845del	NP_001341827.1:p.Asn616MetfsTer5
NM_001354899.2:c.1836del	NP_001341828.1:p.Asn613MetfsTer5
NM_001354900.2:c.1797del	NP_001341829.1:p.Asn600MetfsTer5
NM_001354901.2:c.1743del	NP_001341830.1:p.Asn582MetfsTer5
NM_001354902.2:c.1647del	NP_001341831.1:p.Asn550MetfsTer5
NM_001354903.2:c.1617del	NP_001341832.1:p.Asn540MetfsTer5
NM_001354904.2:c.1542del	NP_001341833.1:p.Asn515MetfsTer5
NM_001354905.2:c.1440del	NP_001341834.1:p.Asn481MetfsTer5
NM_001354906.2:c.1071del	NP_001341835.1:p.Asn358MetfsTer5