Canonical Allele Identifier: CA445963889

Gene: APC

Linked Data

• COSMIC: COSM235669 ; COSM5010344
• MyVariant Identifiers: chr5:g.112175220del (hg19)
• PubMed: PMID:19029688

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839523del , CM000667.2:g.112839523del	GRCh38
NC_000005.9:g.112175220del , CM000667.1:g.112175220del	GRCh37
NC_000005.8:g.112203119del	NCBI36
NG_008481.4:g.152003del , LRG_130:g.152003del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3594del	ENSP00000484935.2:n.3594del
ENST00000504915.3:c.3983del	ENSP00000473355.2:p.Lys1328ArgfsTer11
ENST00000505350.2:c.*3935del	ENSP00000481752.1:n.*3935del
ENST00000507379.6:c.3875del	ENSP00000423224.2:p.Lys1292ArgfsTer11
ENST00000509732.6:c.3929del	ENSP00000426541.2:p.Lys1310ArgfsTer11
ENST00000512211.7:c.3929del	ENSP00000423828.3:p.Lys1310ArgfsTer11
ENST00000257430.9:c.3929del MANE Select	ENSP00000257430.4:p.Lys1310ArgfsTer11
ENST00000257430.8:c.3929del	ENSP00000257430.4:p.Lys1310ArgfsTer11
ENST00000502371.2:c.2282del
ENST00000508376.6:c.3929del	ENSP00000427089.2:p.Lys1310ArgfsTer11
ENST00000508624.5:c.*3251del	ENSP00000424265.1:n.*3251del
ENST00000520401.1:c.230+10551del
NM_000038.5:c.3929del	NP_000029.2:p.Lys1310ArgfsTer11
NM_001127510.2:c.3929del	NP_001120982.1:p.Lys1310ArgfsTer11
NM_001127511.2:c.3875del	NP_001120983.2:p.Lys1292ArgfsTer11
NM_001354895.1:c.3929del	NP_001341824.1:p.Lys1310ArgfsTer11
NM_001354896.1:c.3983del	NP_001341825.1:p.Lys1328ArgfsTer11
NM_001354897.1:c.3959del	NP_001341826.1:p.Lys1320ArgfsTer11
NM_001354898.1:c.3854del	NP_001341827.1:p.Lys1285ArgfsTer11
NM_001354899.1:c.3845del	NP_001341828.1:p.Lys1282ArgfsTer11
NM_001354900.1:c.3806del	NP_001341829.1:p.Lys1269ArgfsTer11
NM_001354901.1:c.3752del	NP_001341830.1:p.Lys1251ArgfsTer11
NM_001354902.1:c.3656del	NP_001341831.1:p.Lys1219ArgfsTer11
NM_001354903.1:c.3626del	NP_001341832.1:p.Lys1209ArgfsTer11
NM_001354904.1:c.3551del	NP_001341833.1:p.Lys1184ArgfsTer11
NM_001354905.1:c.3449del	NP_001341834.1:p.Lys1150ArgfsTer11
NM_001354906.1:c.3080del	NP_001341835.1:p.Lys1027ArgfsTer11
NM_000038.6:c.3929del MANE Select	NP_000029.2:p.Lys1310ArgfsTer11
NM_001127510.3:c.3929del	NP_001120982.1:p.Lys1310ArgfsTer11
NM_001127511.3:c.3875del	NP_001120983.2:p.Lys1292ArgfsTer11
NM_001354895.2:c.3929del	NP_001341824.1:p.Lys1310ArgfsTer11
NM_001354896.2:c.3983del	NP_001341825.1:p.Lys1328ArgfsTer11
NM_001354897.2:c.3959del	NP_001341826.1:p.Lys1320ArgfsTer11
NM_001354898.2:c.3854del	NP_001341827.1:p.Lys1285ArgfsTer11
NM_001354899.2:c.3845del	NP_001341828.1:p.Lys1282ArgfsTer11
NM_001354900.2:c.3806del	NP_001341829.1:p.Lys1269ArgfsTer11
NM_001354901.2:c.3752del	NP_001341830.1:p.Lys1251ArgfsTer11
NM_001354902.2:c.3656del	NP_001341831.1:p.Lys1219ArgfsTer11
NM_001354903.2:c.3626del	NP_001341832.1:p.Lys1209ArgfsTer11
NM_001354904.2:c.3551del	NP_001341833.1:p.Lys1184ArgfsTer11
NM_001354905.2:c.3449del	NP_001341834.1:p.Lys1150ArgfsTer11
NM_001354906.2:c.3080del	NP_001341835.1:p.Lys1027ArgfsTer11