Canonical Allele Identifier: CA2695205031

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828871_112828872del , CM000667.2:g.112828871_112828872del	GRCh38
NC_000005.9:g.112164568_112164569del , CM000667.1:g.112164568_112164569del	GRCh37
NC_000005.8:g.112192467_112192468del	NCBI36
NG_008481.4:g.141351_141352del , LRG_130:g.141351_141352del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6080_1409-6079del	ENSP00000484935.2:n.1409-6080_1409-6079de...
ENST00000504915.3:c.1696_1697del	ENSP00000473355.2:p.Leu566GlufsTer11
ENST00000505084.2:n.1698_1699del
ENST00000505350.2:c.*1648_*1649del	ENSP00000481752.1:n.*1648_*1649del
ENST00000507379.6:c.1588_1589del	ENSP00000423224.2:p.Leu530GlufsTer11
ENST00000509732.6:c.1642_1643del	ENSP00000426541.2:p.Leu548GlufsTer11
ENST00000512211.7:c.1642_1643del	ENSP00000423828.3:p.Leu548GlufsTer11
ENST00000257430.9:c.1642_1643del MANE Select	ENSP00000257430.4:p.Leu548GlufsTer11
ENST00000257430.8:c.1642_1643del	ENSP00000257430.4:p.Leu548GlufsTer11
ENST00000502371.2:c.97-6080_97-6079del
ENST00000504915.2:c.331_332del	ENSP00000473355.1:p.Leu111GlufsTer11
ENST00000505084.1:n.129_130del
ENST00000507379.5:c.1588_1589del	ENSP00000423224.1:p.Leu530GlufsTer11
ENST00000508376.6:c.1642_1643del	ENSP00000427089.2:p.Leu548GlufsTer11
ENST00000508624.5:c.*964_*965del	ENSP00000424265.1:n.*964_*965del
ENST00000512211.6:c.1642_1643del	ENSP00000423828.2:p.Leu548GlufsTer11
ENST00000520401.1:c.129_130del
NM_000038.5:c.1642_1643del	NP_000029.2:p.Leu548GlufsTer11
NM_001127510.2:c.1642_1643del	NP_001120982.1:p.Leu548GlufsTer11
NM_001127511.2:c.1588_1589del	NP_001120983.2:p.Leu530GlufsTer11
NM_001354895.1:c.1642_1643del	NP_001341824.1:p.Leu548GlufsTer11
NM_001354896.1:c.1696_1697del	NP_001341825.1:p.Leu566GlufsTer11
NM_001354897.1:c.1672_1673del	NP_001341826.1:p.Leu558GlufsTer11
NM_001354898.1:c.1567_1568del	NP_001341827.1:p.Leu523GlufsTer11
NM_001354899.1:c.1558_1559del	NP_001341828.1:p.Leu520GlufsTer11
NM_001354900.1:c.1519_1520del	NP_001341829.1:p.Leu507GlufsTer11
NM_001354901.1:c.1465_1466del	NP_001341830.1:p.Leu489GlufsTer11
NM_001354902.1:c.1369_1370del	NP_001341831.1:p.Leu457GlufsTer11
NM_001354903.1:c.1339_1340del	NP_001341832.1:p.Leu447GlufsTer11
NM_001354904.1:c.1264_1265del	NP_001341833.1:p.Leu422GlufsTer11
NM_001354905.1:c.1162_1163del	NP_001341834.1:p.Leu388GlufsTer11
NM_001354906.1:c.793_794del	NP_001341835.1:p.Leu265GlufsTer11
NM_000038.6:c.1642_1643del MANE Select	NP_000029.2:p.Leu548GlufsTer11
NM_001127510.3:c.1642_1643del	NP_001120982.1:p.Leu548GlufsTer11
NM_001127511.3:c.1588_1589del	NP_001120983.2:p.Leu530GlufsTer11
NM_001354895.2:c.1642_1643del	NP_001341824.1:p.Leu548GlufsTer11
NM_001354896.2:c.1696_1697del	NP_001341825.1:p.Leu566GlufsTer11
NM_001354897.2:c.1672_1673del	NP_001341826.1:p.Leu558GlufsTer11
NM_001354898.2:c.1567_1568del	NP_001341827.1:p.Leu523GlufsTer11
NM_001354899.2:c.1558_1559del	NP_001341828.1:p.Leu520GlufsTer11
NM_001354900.2:c.1519_1520del	NP_001341829.1:p.Leu507GlufsTer11
NM_001354901.2:c.1465_1466del	NP_001341830.1:p.Leu489GlufsTer11
NM_001354902.2:c.1369_1370del	NP_001341831.1:p.Leu457GlufsTer11
NM_001354903.2:c.1339_1340del	NP_001341832.1:p.Leu447GlufsTer11
NM_001354904.2:c.1264_1265del	NP_001341833.1:p.Leu422GlufsTer11
NM_001354905.2:c.1162_1163del	NP_001341834.1:p.Leu388GlufsTer11
NM_001354906.2:c.793_794del	NP_001341835.1:p.Leu265GlufsTer11