Canonical Allele Identifier: CA445960347

Gene: APC

Linked Data

• COSMIC: COSM19207
• MyVariant Identifiers: chr5:g.112154936del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819239del , CM000667.2:g.112819239del	GRCh38
NC_000005.9:g.112154936del , CM000667.1:g.112154936del	GRCh37
NC_000005.8:g.112182835del	NCBI36
NG_008481.4:g.131719del , LRG_130:g.131719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1207del	ENSP00000484935.2:p.Glu403LysfsTer?
ENST00000504915.3:c.1207del	ENSP00000473355.2:p.Glu403LysfsTer?
ENST00000505084.2:n.1263del
ENST00000505350.2:c.*1213del	ENSP00000481752.1:n.*1213del
ENST00000507379.6:c.1153del	ENSP00000423224.2:p.Glu385LysfsTer?
ENST00000509732.6:c.1207del	ENSP00000426541.2:p.Glu403LysfsTer?
ENST00000512211.7:c.1207del	ENSP00000423828.3:p.Glu403LysfsTer?
ENST00000257430.9:c.1207del MANE Select	ENSP00000257430.4:p.Glu403LysfsTer?
ENST00000257430.8:c.1207del	ENSP00000257430.4:p.Glu403LysfsTer?
ENST00000507379.5:c.1153del	ENSP00000423224.1:p.Glu385LysfsTer?
ENST00000508376.6:c.1207del	ENSP00000427089.2:p.Glu403LysfsTer?
ENST00000508624.5:c.*529del	ENSP00000424265.1:n.*529del
ENST00000512211.6:c.1207del	ENSP00000423828.2:p.Glu403LysfsTer?
NM_000038.5:c.1207del	NP_000029.2:p.Glu403LysfsTer?
NM_001127510.2:c.1207del	NP_001120982.1:p.Glu403LysfsTer?
NM_001127511.2:c.1153del	NP_001120983.2:p.Glu385LysfsTer?
NM_001354895.1:c.1207del	NP_001341824.1:p.Glu403LysfsTer?
NM_001354896.1:c.1207del	NP_001341825.1:p.Glu403LysfsTer?
NM_001354897.1:c.1237del	NP_001341826.1:p.Glu413LysfsTer?
NM_001354898.1:c.1132del	NP_001341827.1:p.Glu378LysfsTer?
NM_001354899.1:c.1123del	NP_001341828.1:p.Glu375LysfsTer?
NM_001354900.1:c.1030del	NP_001341829.1:p.Glu344LysfsTer?
NM_001354901.1:c.1030del	NP_001341830.1:p.Glu344LysfsTer?
NM_001354902.1:c.964-30del	NP_001341831.1:n.964-30del
NM_001354903.1:c.934-30del	NP_001341832.1:n.934-30del
NM_001354904.1:c.859-30del	NP_001341833.1:n.859-30del
NM_001354905.1:c.757-30del	NP_001341834.1:n.757-30del
NM_001354906.1:c.358del	NP_001341835.1:p.Glu120LysfsTer?
NM_000038.6:c.1207del MANE Select	NP_000029.2:p.Glu403LysfsTer?
NM_001127510.3:c.1207del	NP_001120982.1:p.Glu403LysfsTer?
NM_001127511.3:c.1153del	NP_001120983.2:p.Glu385LysfsTer?
NM_001354895.2:c.1207del	NP_001341824.1:p.Glu403LysfsTer?
NM_001354896.2:c.1207del	NP_001341825.1:p.Glu403LysfsTer?
NM_001354897.2:c.1237del	NP_001341826.1:p.Glu413LysfsTer?
NM_001354898.2:c.1132del	NP_001341827.1:p.Glu378LysfsTer?
NM_001354899.2:c.1123del	NP_001341828.1:p.Glu375LysfsTer?
NM_001354900.2:c.1030del	NP_001341829.1:p.Glu344LysfsTer?
NM_001354901.2:c.1030del	NP_001341830.1:p.Glu344LysfsTer?
NM_001354902.2:c.964-30del	NP_001341831.1:n.964-30del
NM_001354903.2:c.934-30del	NP_001341832.1:n.934-30del
NM_001354904.2:c.859-30del	NP_001341833.1:n.859-30del
NM_001354905.2:c.757-30del	NP_001341834.1:n.757-30del
NM_001354906.2:c.358del	NP_001341835.1:p.Glu120LysfsTer?