Canonical Allele Identifier: CA658760521

Gene: APC

Linked Data

• PubMed: PMID:11247896

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828930_112828934del , CM000667.2:g.112828930_112828934del	GRCh38
NC_000005.9:g.112164627_112164631del , CM000667.1:g.112164627_112164631del	GRCh37
NC_000005.8:g.112192526_112192530del	NCBI36
NG_008481.4:g.141410_141414del , LRG_130:g.141410_141414del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1409-6021_1409-6017del	ENSP00000484935.2:n.1409-6021_1409-6017del
ENST00000504915.3:c.1755_1759del	ENSP00000473355.2:p.Ser586GlufsTer11
ENST00000505084.2:n.1757_1761del
ENST00000505350.2:c.*1707_*1711del	ENSP00000481752.1:n.*1707_*1711del
ENST00000507379.6:c.1647_1651del	ENSP00000423224.2:p.Ser550GlufsTer11
ENST00000509732.6:c.1701_1705del	ENSP00000426541.2:p.Ser568GlufsTer11
ENST00000512211.7:c.1701_1705del	ENSP00000423828.3:p.Ser568GlufsTer11
ENST00000257430.9:c.1701_1705del MANE Select	ENSP00000257430.4:p.Ser568GlufsTer11
ENST00000257430.8:c.1701_1705del	ENSP00000257430.4:p.Ser568GlufsTer11
ENST00000502371.2:c.97-6021_97-6017del
ENST00000504915.2:c.390_394del	ENSP00000473355.1:p.Ser131GlufsTer11
ENST00000505084.1:n.188_192del
ENST00000507379.5:c.1647_1651del	ENSP00000423224.1:p.Ser550GlufsTer11
ENST00000508376.6:c.1701_1705del	ENSP00000427089.2:p.Ser568GlufsTer11
ENST00000508624.5:c.*1023_*1027del	ENSP00000424265.1:n.*1023_*1027del
ENST00000512211.6:c.1701_1705del	ENSP00000423828.2:p.Ser568GlufsTer11
ENST00000520401.1:c.188_192del
NM_000038.5:c.1701_1705del	NP_000029.2:p.Ser568GlufsTer11
NM_001127510.2:c.1701_1705del	NP_001120982.1:p.Ser568GlufsTer11
NM_001127511.2:c.1647_1651del	NP_001120983.2:p.Ser550GlufsTer11
NM_001354895.1:c.1701_1705del	NP_001341824.1:p.Ser568GlufsTer11
NM_001354896.1:c.1755_1759del	NP_001341825.1:p.Ser586GlufsTer11
NM_001354897.1:c.1731_1735del	NP_001341826.1:p.Ser578GlufsTer11
NM_001354898.1:c.1626_1630del	NP_001341827.1:p.Ser543GlufsTer11
NM_001354899.1:c.1617_1621del	NP_001341828.1:p.Ser540GlufsTer11
NM_001354900.1:c.1578_1582del	NP_001341829.1:p.Ser527GlufsTer11
NM_001354901.1:c.1524_1528del	NP_001341830.1:p.Ser509GlufsTer11
NM_001354902.1:c.1428_1432del	NP_001341831.1:p.Ser477GlufsTer11
NM_001354903.1:c.1398_1402del	NP_001341832.1:p.Ser467GlufsTer11
NM_001354904.1:c.1323_1327del	NP_001341833.1:p.Ser442GlufsTer11
NM_001354905.1:c.1221_1225del	NP_001341834.1:p.Ser408GlufsTer11
NM_001354906.1:c.852_856del	NP_001341835.1:p.Ser285GlufsTer11
NM_000038.6:c.1701_1705del MANE Select	NP_000029.2:p.Ser568GlufsTer11
NM_001127510.3:c.1701_1705del	NP_001120982.1:p.Ser568GlufsTer11
NM_001127511.3:c.1647_1651del	NP_001120983.2:p.Ser550GlufsTer11
NM_001354895.2:c.1701_1705del	NP_001341824.1:p.Ser568GlufsTer11
NM_001354896.2:c.1755_1759del	NP_001341825.1:p.Ser586GlufsTer11
NM_001354897.2:c.1731_1735del	NP_001341826.1:p.Ser578GlufsTer11
NM_001354898.2:c.1626_1630del	NP_001341827.1:p.Ser543GlufsTer11
NM_001354899.2:c.1617_1621del	NP_001341828.1:p.Ser540GlufsTer11
NM_001354900.2:c.1578_1582del	NP_001341829.1:p.Ser527GlufsTer11
NM_001354901.2:c.1524_1528del	NP_001341830.1:p.Ser509GlufsTer11
NM_001354902.2:c.1428_1432del	NP_001341831.1:p.Ser477GlufsTer11
NM_001354903.2:c.1398_1402del	NP_001341832.1:p.Ser467GlufsTer11
NM_001354904.2:c.1323_1327del	NP_001341833.1:p.Ser442GlufsTer11
NM_001354905.2:c.1221_1225del	NP_001341834.1:p.Ser408GlufsTer11
NM_001354906.2:c.852_856del	NP_001341835.1:p.Ser285GlufsTer11