Canonical Allele Identifier: CA658760869

Gene: APC

Linked Data

• PubMed: PMID:11247896

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838665del , CM000667.2:g.112838665del	GRCh38
NC_000005.9:g.112174362del , CM000667.1:g.112174362del	GRCh37
NC_000005.8:g.112202261del	NCBI36
NG_008481.4:g.151145del , LRG_130:g.151145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2736del	ENSP00000484935.2:n.2736del
ENST00000504915.3:c.3125del	ENSP00000473355.2:p.Pro1042GlnfsTer2
ENST00000505350.2:c.*3077del	ENSP00000481752.1:n.*3077del
ENST00000507379.6:c.3017del	ENSP00000423224.2:p.Pro1006GlnfsTer2
ENST00000509732.6:c.3071del	ENSP00000426541.2:p.Pro1024GlnfsTer2
ENST00000512211.7:c.3071del	ENSP00000423828.3:p.Pro1024GlnfsTer2
ENST00000257430.9:c.3071del MANE Select	ENSP00000257430.4:p.Pro1024GlnfsTer2
ENST00000257430.8:c.3071del	ENSP00000257430.4:p.Pro1024GlnfsTer2
ENST00000502371.2:c.1424del
ENST00000507379.5:c.3017del	ENSP00000423224.1:p.Pro1006GlnfsTer2
ENST00000508376.6:c.3071del	ENSP00000427089.2:p.Pro1024GlnfsTer2
ENST00000508624.5:c.*2393del	ENSP00000424265.1:n.*2393del
ENST00000512211.6:c.3071del	ENSP00000423828.2:p.Pro1024GlnfsTer2
ENST00000520401.1:c.230+9693del
NM_000038.5:c.3071del	NP_000029.2:p.Pro1024GlnfsTer2
NM_001127510.2:c.3071del	NP_001120982.1:p.Pro1024GlnfsTer2
NM_001127511.2:c.3017del	NP_001120983.2:p.Pro1006GlnfsTer2
NM_001354895.1:c.3071del	NP_001341824.1:p.Pro1024GlnfsTer2
NM_001354896.1:c.3125del	NP_001341825.1:p.Pro1042GlnfsTer2
NM_001354897.1:c.3101del	NP_001341826.1:p.Pro1034GlnfsTer2
NM_001354898.1:c.2996del	NP_001341827.1:p.Pro999GlnfsTer2
NM_001354899.1:c.2987del	NP_001341828.1:p.Pro996GlnfsTer2
NM_001354900.1:c.2948del	NP_001341829.1:p.Pro983GlnfsTer2
NM_001354901.1:c.2894del	NP_001341830.1:p.Pro965GlnfsTer2
NM_001354902.1:c.2798del	NP_001341831.1:p.Pro933GlnfsTer2
NM_001354903.1:c.2768del	NP_001341832.1:p.Pro923GlnfsTer2
NM_001354904.1:c.2693del	NP_001341833.1:p.Pro898GlnfsTer2
NM_001354905.1:c.2591del	NP_001341834.1:p.Pro864GlnfsTer2
NM_001354906.1:c.2222del	NP_001341835.1:p.Pro741GlnfsTer2
NM_000038.6:c.3071del MANE Select	NP_000029.2:p.Pro1024GlnfsTer2
NM_001127510.3:c.3071del	NP_001120982.1:p.Pro1024GlnfsTer2
NM_001127511.3:c.3017del	NP_001120983.2:p.Pro1006GlnfsTer2
NM_001354895.2:c.3071del	NP_001341824.1:p.Pro1024GlnfsTer2
NM_001354896.2:c.3125del	NP_001341825.1:p.Pro1042GlnfsTer2
NM_001354897.2:c.3101del	NP_001341826.1:p.Pro1034GlnfsTer2
NM_001354898.2:c.2996del	NP_001341827.1:p.Pro999GlnfsTer2
NM_001354899.2:c.2987del	NP_001341828.1:p.Pro996GlnfsTer2
NM_001354900.2:c.2948del	NP_001341829.1:p.Pro983GlnfsTer2
NM_001354901.2:c.2894del	NP_001341830.1:p.Pro965GlnfsTer2
NM_001354902.2:c.2798del	NP_001341831.1:p.Pro933GlnfsTer2
NM_001354903.2:c.2768del	NP_001341832.1:p.Pro923GlnfsTer2
NM_001354904.2:c.2693del	NP_001341833.1:p.Pro898GlnfsTer2
NM_001354905.2:c.2591del	NP_001341834.1:p.Pro864GlnfsTer2
NM_001354906.2:c.2222del	NP_001341835.1:p.Pro741GlnfsTer2