Canonical Allele Identifier: CA445758843

Gene: APC

Linked Data

• COSMIC: COSM235660
• MyVariant Identifiers: chr5:g.112170701del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835004del , CM000667.2:g.112835004del	GRCh38
NC_000005.9:g.112170701del , CM000667.1:g.112170701del	GRCh37
NC_000005.8:g.112198600del	NCBI36
NG_008481.4:g.147484del , LRG_130:g.147484del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1462del	ENSP00000484935.2:p.His488ThrfsTer?
ENST00000504915.3:c.1851del	ENSP00000473355.2:p.Cys617Ter
ENST00000505350.2:c.*1803del	ENSP00000481752.1:n.*1803del
ENST00000507379.6:c.1743del	ENSP00000423224.2:p.Cys581Ter
ENST00000509732.6:c.1797del	ENSP00000426541.2:p.Cys599Ter
ENST00000512211.7:c.1797del	ENSP00000423828.3:p.Cys599Ter
ENST00000257430.9:c.1797del MANE Select	ENSP00000257430.4:p.Cys599Ter
ENST00000257430.8:c.1797del	ENSP00000257430.4:p.Cys599Ter
ENST00000502371.2:c.150del
ENST00000504915.2:c.486del	ENSP00000473355.1:p.Cys162Ter
ENST00000507379.5:c.1743del	ENSP00000423224.1:p.Cys581Ter
ENST00000508376.6:c.1797del	ENSP00000427089.2:p.Cys599Ter
ENST00000508624.5:c.*1119del	ENSP00000424265.1:n.*1119del
ENST00000512211.6:c.1797del	ENSP00000423828.2:p.Cys599Ter
ENST00000520401.1:c.230+6032del
NM_000038.5:c.1797del	NP_000029.2:p.Cys599Ter
NM_001127510.2:c.1797del	NP_001120982.1:p.Cys599Ter
NM_001127511.2:c.1743del	NP_001120983.2:p.Cys581Ter
NM_001354895.1:c.1797del	NP_001341824.1:p.Cys599Ter
NM_001354896.1:c.1851del	NP_001341825.1:p.Cys617Ter
NM_001354897.1:c.1827del	NP_001341826.1:p.Cys609Ter
NM_001354898.1:c.1722del	NP_001341827.1:p.Cys574Ter
NM_001354899.1:c.1713del	NP_001341828.1:p.Cys571Ter
NM_001354900.1:c.1674del	NP_001341829.1:p.Cys558Ter
NM_001354901.1:c.1620del	NP_001341830.1:p.Cys540Ter
NM_001354902.1:c.1524del	NP_001341831.1:p.Cys508Ter
NM_001354903.1:c.1494del	NP_001341832.1:p.Cys498Ter
NM_001354904.1:c.1419del	NP_001341833.1:p.Cys473Ter
NM_001354905.1:c.1317del	NP_001341834.1:p.Cys439Ter
NM_001354906.1:c.948del	NP_001341835.1:p.Cys316Ter
NM_000038.6:c.1797del MANE Select	NP_000029.2:p.Cys599Ter
NM_001127510.3:c.1797del	NP_001120982.1:p.Cys599Ter
NM_001127511.3:c.1743del	NP_001120983.2:p.Cys581Ter
NM_001354895.2:c.1797del	NP_001341824.1:p.Cys599Ter
NM_001354896.2:c.1851del	NP_001341825.1:p.Cys617Ter
NM_001354897.2:c.1827del	NP_001341826.1:p.Cys609Ter
NM_001354898.2:c.1722del	NP_001341827.1:p.Cys574Ter
NM_001354899.2:c.1713del	NP_001341828.1:p.Cys571Ter
NM_001354900.2:c.1674del	NP_001341829.1:p.Cys558Ter
NM_001354901.2:c.1620del	NP_001341830.1:p.Cys540Ter
NM_001354902.2:c.1524del	NP_001341831.1:p.Cys508Ter
NM_001354903.2:c.1494del	NP_001341832.1:p.Cys498Ter
NM_001354904.2:c.1419del	NP_001341833.1:p.Cys473Ter
NM_001354905.2:c.1317del	NP_001341834.1:p.Cys439Ter
NM_001354906.2:c.948del	NP_001341835.1:p.Cys316Ter