Canonical Allele Identifier: CA658760630

Gene: APC

Linked Data

• PubMed: PMID:15857185

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835153_112835154insG , CM000667.2:g.112835153_112835154insG	GRCh38
NC_000005.9:g.112170850_112170851insG , CM000667.1:g.112170850_112170851insG	GRCh37
NC_000005.8:g.112198749_112198750insG	NCBI36
NG_008481.4:g.147633_147634insG , LRG_130:g.147633_147634insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1611_1612insG	ENSP00000484935.2:n.1611_1612insG
ENST00000504915.3:c.2000_2001insG	ENSP00000473355.2:p.Asn667LysfsTer2
ENST00000505350.2:c.*1952_*1953insG	ENSP00000481752.1:n.*1952_*1953insG
ENST00000507379.6:c.1892_1893insG	ENSP00000423224.2:p.Asn631LysfsTer2
ENST00000509732.6:c.1946_1947insG	ENSP00000426541.2:p.Asn649LysfsTer2
ENST00000512211.7:c.1946_1947insG	ENSP00000423828.3:p.Asn649LysfsTer2
ENST00000257430.9:c.1946_1947insG MANE Select	ENSP00000257430.4:p.Asn649LysfsTer2
ENST00000257430.8:c.1946_1947insG	ENSP00000257430.4:p.Asn649LysfsTer2
ENST00000502371.2:c.299_300insG
ENST00000504915.2:c.635_636insG	ENSP00000473355.1:p.Asn212LysfsTer2
ENST00000507379.5:c.1892_1893insG	ENSP00000423224.1:p.Asn631LysfsTer2
ENST00000508376.6:c.1946_1947insG	ENSP00000427089.2:p.Asn649LysfsTer2
ENST00000508624.5:c.*1268_*1269insG	ENSP00000424265.1:n.*1268_*1269insG
ENST00000512211.6:c.1946_1947insG	ENSP00000423828.2:p.Asn649LysfsTer2
ENST00000520401.1:c.230+6181_230+6182insG
NM_000038.5:c.1946_1947insG	NP_000029.2:p.Asn649LysfsTer2
NM_001127510.2:c.1946_1947insG	NP_001120982.1:p.Asn649LysfsTer2
NM_001127511.2:c.1892_1893insG	NP_001120983.2:p.Asn631LysfsTer2
NM_001354895.1:c.1946_1947insG	NP_001341824.1:p.Asn649LysfsTer2
NM_001354896.1:c.2000_2001insG	NP_001341825.1:p.Asn667LysfsTer2
NM_001354897.1:c.1976_1977insG	NP_001341826.1:p.Asn659LysfsTer2
NM_001354898.1:c.1871_1872insG	NP_001341827.1:p.Asn624LysfsTer2
NM_001354899.1:c.1862_1863insG	NP_001341828.1:p.Asn621LysfsTer2
NM_001354900.1:c.1823_1824insG	NP_001341829.1:p.Asn608LysfsTer2
NM_001354901.1:c.1769_1770insG	NP_001341830.1:p.Asn590LysfsTer2
NM_001354902.1:c.1673_1674insG	NP_001341831.1:p.Asn558LysfsTer2
NM_001354903.1:c.1643_1644insG	NP_001341832.1:p.Asn548LysfsTer2
NM_001354904.1:c.1568_1569insG	NP_001341833.1:p.Asn523LysfsTer2
NM_001354905.1:c.1466_1467insG	NP_001341834.1:p.Asn489LysfsTer2
NM_001354906.1:c.1097_1098insG	NP_001341835.1:p.Asn366LysfsTer2
NM_000038.6:c.1946_1947insG MANE Select	NP_000029.2:p.Asn649LysfsTer2
NM_001127510.3:c.1946_1947insG	NP_001120982.1:p.Asn649LysfsTer2
NM_001127511.3:c.1892_1893insG	NP_001120983.2:p.Asn631LysfsTer2
NM_001354895.2:c.1946_1947insG	NP_001341824.1:p.Asn649LysfsTer2
NM_001354896.2:c.2000_2001insG	NP_001341825.1:p.Asn667LysfsTer2
NM_001354897.2:c.1976_1977insG	NP_001341826.1:p.Asn659LysfsTer2
NM_001354898.2:c.1871_1872insG	NP_001341827.1:p.Asn624LysfsTer2
NM_001354899.2:c.1862_1863insG	NP_001341828.1:p.Asn621LysfsTer2
NM_001354900.2:c.1823_1824insG	NP_001341829.1:p.Asn608LysfsTer2
NM_001354901.2:c.1769_1770insG	NP_001341830.1:p.Asn590LysfsTer2
NM_001354902.2:c.1673_1674insG	NP_001341831.1:p.Asn558LysfsTer2
NM_001354903.2:c.1643_1644insG	NP_001341832.1:p.Asn548LysfsTer2
NM_001354904.2:c.1568_1569insG	NP_001341833.1:p.Asn523LysfsTer2
NM_001354905.2:c.1466_1467insG	NP_001341834.1:p.Asn489LysfsTer2
NM_001354906.2:c.1097_1098insG	NP_001341835.1:p.Asn366LysfsTer2