Canonical Allele Identifier: CA2674863811

Gene: APC

Linked Data

• gnomAD v4: 5-112737933-CTGGAGCCACCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737937_112737947del , CM000667.2:g.112737937_112737947del	GRCh38
NC_000005.9:g.112073634_112073644del , CM000667.1:g.112073634_112073644del	GRCh37
NC_000005.8:g.112101533_112101543del	NCBI36
NG_008481.4:g.50417_50427del , LRG_130:g.50417_50427del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.-19+12_-19+22del	ENSP00000473355.2:n.-19+12_-19+22del
ENST00000505084.2:n.38+12_38+22del
ENST00000505350.2:c.166-16936_166-16926del	ENSP00000481752.1:n.166-16936_166-16926del
ENST00000507379.6:c.166-28389_166-28379del	ENSP00000423224.2:n.166-28389_166-28379del
ENST00000509732.6:c.-18-16936_-18-16926del	ENSP00000426541.2:n.-18-16936_-18-16926del
ENST00000257430.9:c.-19+12_-19+22del MANE Select	ENSP00000257430.4:n.-19+12_-19+22del
ENST00000257430.8:c.-19+12_-19+22del	ENSP00000257430.4:n.-19+12_-19+22del
ENST00000505350.1:c.166-16936_166-16926del	ENSP00000481752.1:n.166-16936_166-16926del
ENST00000507379.5:c.166-28389_166-28379del	ENSP00000423224.1:n.166-28389_166-28379del
ENST00000508376.6:c.-127+12_-127+22del	ENSP00000427089.2:n.-127+12_-127+22del
ENST00000508624.5:c.-19+12_-19+22del	ENSP00000424265.1:n.-19+12_-19+22del
ENST00000509732.5:c.-18-16936_-18-16926del	ENSP00000426541.1:n.-18-16936_-18-16926del
NM_000038.5:c.-19+12_-19+22del	NP_000029.2:n.-19+12_-19+22del
NM_001127510.2:c.-127+12_-127+22del	NP_001120982.1:n.-127+12_-127+22del
NM_001127511.2:c.166-28389_166-28379del	NP_001120983.2:n.166-28389_166-28379del
NM_001354895.1:c.-18-16936_-18-16926del	NP_001341824.1:n.-18-16936_-18-16926del
NM_001354896.1:c.-19+12_-19+22del	NP_001341825.1:n.-19+12_-19+22del
NM_001354897.1:c.166-28389_166-28379del	NP_001341826.1:n.166-28389_166-28379del
NM_001354898.1:c.-49+12_-49+22del	NP_001341827.1:n.-49+12_-49+22del
NM_001354899.1:c.-19+12_-19+22del	NP_001341828.1:n.-19+12_-19+22del
NM_001354900.1:c.-43+12_-43+22del	NP_001341829.1:n.-43+12_-43+22del
NM_001354901.1:c.-43+12_-43+22del	NP_001341830.1:n.-43+12_-43+22del
NM_001354902.1:c.166-28389_166-28379del	NP_001341831.1:n.166-28389_166-28379del
NM_001354903.1:c.-19+12_-19+22del	NP_001341832.1:n.-19+12_-19+22del
NM_001354904.1:c.-49+12_-49+22del	NP_001341833.1:n.-49+12_-49+22del
NM_001354905.1:c.-43+12_-43+22del	NP_001341834.1:n.-43+12_-43+22del
NM_001354906.1:c.-1054+12_-1054+22del	NP_001341835.1:n.-1054+12_-1054+22del
NM_000038.6:c.-19+12_-19+22del MANE Select	NP_000029.2:n.-19+12_-19+22del
NM_001127510.3:c.-127+12_-127+22del	NP_001120982.1:n.-127+12_-127+22del
NM_001127511.3:c.166-28389_166-28379del	NP_001120983.2:n.166-28389_166-28379del
NM_001354895.2:c.-18-16936_-18-16926del	NP_001341824.1:n.-18-16936_-18-16926del
NM_001354896.2:c.-19+12_-19+22del	NP_001341825.1:n.-19+12_-19+22del
NM_001354897.2:c.166-28389_166-28379del	NP_001341826.1:n.166-28389_166-28379del
NM_001354898.2:c.-49+12_-49+22del	NP_001341827.1:n.-49+12_-49+22del
NM_001354899.2:c.-19+12_-19+22del	NP_001341828.1:n.-19+12_-19+22del
NM_001354900.2:c.-43+12_-43+22del	NP_001341829.1:n.-43+12_-43+22del
NM_001354901.2:c.-43+12_-43+22del	NP_001341830.1:n.-43+12_-43+22del
NM_001354902.2:c.166-28389_166-28379del	NP_001341831.1:n.166-28389_166-28379del
NM_001354903.2:c.-19+12_-19+22del	NP_001341832.1:n.-19+12_-19+22del
NM_001354904.2:c.-49+12_-49+22del	NP_001341833.1:n.-49+12_-49+22del
NM_001354905.2:c.-43+12_-43+22del	NP_001341834.1:n.-43+12_-43+22del
NM_001354906.2:c.-1054+12_-1054+22del	NP_001341835.1:n.-1054+12_-1054+22del