Canonical Allele Identifier: CA658760912

Gene: APC

Linked Data

• PubMed: PMID:19029688

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838965del , CM000667.2:g.112838965del	GRCh38
NC_000005.9:g.112174662del , CM000667.1:g.112174662del	GRCh37
NC_000005.8:g.112202561del	NCBI36
NG_008481.4:g.151445del , LRG_130:g.151445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3036del	ENSP00000484935.2:n.3036del
ENST00000504915.3:c.3425del	ENSP00000473355.2:p.Asn1142MetfsTer2
ENST00000505350.2:c.*3377del	ENSP00000481752.1:n.*3377del
ENST00000507379.6:c.3317del	ENSP00000423224.2:p.Asn1106MetfsTer2
ENST00000509732.6:c.3371del	ENSP00000426541.2:p.Asn1124MetfsTer2
ENST00000512211.7:c.3371del	ENSP00000423828.3:p.Asn1124MetfsTer2
ENST00000257430.9:c.3371del MANE Select	ENSP00000257430.4:p.Asn1124MetfsTer2
ENST00000257430.8:c.3371del	ENSP00000257430.4:p.Asn1124MetfsTer2
ENST00000502371.2:c.1724del
ENST00000507379.5:c.3317del	ENSP00000423224.1:p.Asn1106MetfsTer2
ENST00000508376.6:c.3371del	ENSP00000427089.2:p.Asn1124MetfsTer2
ENST00000508624.5:c.*2693del	ENSP00000424265.1:n.*2693del
ENST00000512211.6:c.3371del	ENSP00000423828.2:p.Asn1124MetfsTer2
ENST00000520401.1:c.230+9993del
NM_000038.5:c.3371del	NP_000029.2:p.Asn1124MetfsTer2
NM_001127510.2:c.3371del	NP_001120982.1:p.Asn1124MetfsTer2
NM_001127511.2:c.3317del	NP_001120983.2:p.Asn1106MetfsTer2
NM_001354895.1:c.3371del	NP_001341824.1:p.Asn1124MetfsTer2
NM_001354896.1:c.3425del	NP_001341825.1:p.Asn1142MetfsTer2
NM_001354897.1:c.3401del	NP_001341826.1:p.Asn1134MetfsTer2
NM_001354898.1:c.3296del	NP_001341827.1:p.Asn1099MetfsTer2
NM_001354899.1:c.3287del	NP_001341828.1:p.Asn1096MetfsTer2
NM_001354900.1:c.3248del	NP_001341829.1:p.Asn1083MetfsTer2
NM_001354901.1:c.3194del	NP_001341830.1:p.Asn1065MetfsTer2
NM_001354902.1:c.3098del	NP_001341831.1:p.Asn1033MetfsTer2
NM_001354903.1:c.3068del	NP_001341832.1:p.Asn1023MetfsTer2
NM_001354904.1:c.2993del	NP_001341833.1:p.Asn998MetfsTer2
NM_001354905.1:c.2891del	NP_001341834.1:p.Asn964MetfsTer2
NM_001354906.1:c.2522del	NP_001341835.1:p.Asn841MetfsTer2
NM_000038.6:c.3371del MANE Select	NP_000029.2:p.Asn1124MetfsTer2
NM_001127510.3:c.3371del	NP_001120982.1:p.Asn1124MetfsTer2
NM_001127511.3:c.3317del	NP_001120983.2:p.Asn1106MetfsTer2
NM_001354895.2:c.3371del	NP_001341824.1:p.Asn1124MetfsTer2
NM_001354896.2:c.3425del	NP_001341825.1:p.Asn1142MetfsTer2
NM_001354897.2:c.3401del	NP_001341826.1:p.Asn1134MetfsTer2
NM_001354898.2:c.3296del	NP_001341827.1:p.Asn1099MetfsTer2
NM_001354899.2:c.3287del	NP_001341828.1:p.Asn1096MetfsTer2
NM_001354900.2:c.3248del	NP_001341829.1:p.Asn1083MetfsTer2
NM_001354901.2:c.3194del	NP_001341830.1:p.Asn1065MetfsTer2
NM_001354902.2:c.3098del	NP_001341831.1:p.Asn1033MetfsTer2
NM_001354903.2:c.3068del	NP_001341832.1:p.Asn1023MetfsTer2
NM_001354904.2:c.2993del	NP_001341833.1:p.Asn998MetfsTer2
NM_001354905.2:c.2891del	NP_001341834.1:p.Asn964MetfsTer2
NM_001354906.2:c.2522del	NP_001341835.1:p.Asn841MetfsTer2