Canonical Allele Identifier: CA445963163

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112174366del (hg19)
• PubMed: PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838671del , CM000667.2:g.112838671del	GRCh38
NC_000005.9:g.112174368del , CM000667.1:g.112174368del	GRCh37
NC_000005.8:g.112202267del	NCBI36
NG_008481.4:g.151151del , LRG_130:g.151151del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2742del	ENSP00000484935.2:n.2742del
ENST00000504915.3:c.3131del	ENSP00000473355.2:p.Asn1044IlefsTer11
ENST00000505350.2:c.*3083del	ENSP00000481752.1:n.*3083del
ENST00000507379.6:c.3023del	ENSP00000423224.2:p.Asn1008IlefsTer11
ENST00000509732.6:c.3077del	ENSP00000426541.2:p.Asn1026IlefsTer11
ENST00000512211.7:c.3077del	ENSP00000423828.3:p.Asn1026IlefsTer11
ENST00000257430.9:c.3077del MANE Select	ENSP00000257430.4:p.Asn1026IlefsTer11
ENST00000257430.8:c.3077del	ENSP00000257430.4:p.Asn1026IlefsTer11
ENST00000502371.2:c.1430del
ENST00000507379.5:c.3023del	ENSP00000423224.1:p.Asn1008IlefsTer11
ENST00000508376.6:c.3077del	ENSP00000427089.2:p.Asn1026IlefsTer11
ENST00000508624.5:c.*2399del	ENSP00000424265.1:n.*2399del
ENST00000512211.6:c.3077del	ENSP00000423828.2:p.Asn1026IlefsTer11
ENST00000520401.1:c.230+9699del
NM_000038.5:c.3077del	NP_000029.2:p.Asn1026IlefsTer11
NM_001127510.2:c.3077del	NP_001120982.1:p.Asn1026IlefsTer11
NM_001127511.2:c.3023del	NP_001120983.2:p.Asn1008IlefsTer11
NM_001354895.1:c.3077del	NP_001341824.1:p.Asn1026IlefsTer11
NM_001354896.1:c.3131del	NP_001341825.1:p.Asn1044IlefsTer11
NM_001354897.1:c.3107del	NP_001341826.1:p.Asn1036IlefsTer11
NM_001354898.1:c.3002del	NP_001341827.1:p.Asn1001IlefsTer11
NM_001354899.1:c.2993del	NP_001341828.1:p.Asn998IlefsTer11
NM_001354900.1:c.2954del	NP_001341829.1:p.Asn985IlefsTer11
NM_001354901.1:c.2900del	NP_001341830.1:p.Asn967IlefsTer11
NM_001354902.1:c.2804del	NP_001341831.1:p.Asn935IlefsTer11
NM_001354903.1:c.2774del	NP_001341832.1:p.Asn925IlefsTer11
NM_001354904.1:c.2699del	NP_001341833.1:p.Asn900IlefsTer11
NM_001354905.1:c.2597del	NP_001341834.1:p.Asn866IlefsTer11
NM_001354906.1:c.2228del	NP_001341835.1:p.Asn743IlefsTer11
NM_000038.6:c.3077del MANE Select	NP_000029.2:p.Asn1026IlefsTer11
NM_001127510.3:c.3077del	NP_001120982.1:p.Asn1026IlefsTer11
NM_001127511.3:c.3023del	NP_001120983.2:p.Asn1008IlefsTer11
NM_001354895.2:c.3077del	NP_001341824.1:p.Asn1026IlefsTer11
NM_001354896.2:c.3131del	NP_001341825.1:p.Asn1044IlefsTer11
NM_001354897.2:c.3107del	NP_001341826.1:p.Asn1036IlefsTer11
NM_001354898.2:c.3002del	NP_001341827.1:p.Asn1001IlefsTer11
NM_001354899.2:c.2993del	NP_001341828.1:p.Asn998IlefsTer11
NM_001354900.2:c.2954del	NP_001341829.1:p.Asn985IlefsTer11
NM_001354901.2:c.2900del	NP_001341830.1:p.Asn967IlefsTer11
NM_001354902.2:c.2804del	NP_001341831.1:p.Asn935IlefsTer11
NM_001354903.2:c.2774del	NP_001341832.1:p.Asn925IlefsTer11
NM_001354904.2:c.2699del	NP_001341833.1:p.Asn900IlefsTer11
NM_001354905.2:c.2597del	NP_001341834.1:p.Asn866IlefsTer11
NM_001354906.2:c.2228del	NP_001341835.1:p.Asn743IlefsTer11