Canonical Allele Identifier: CA2674863843

Gene: APC

Linked Data

• gnomAD v4: 5-112737964-GGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737967_112737969del , CM000667.2:g.112737967_112737969del	GRCh38
NC_000005.9:g.112073664_112073666del , CM000667.1:g.112073664_112073666del	GRCh37
NC_000005.8:g.112101563_112101565del	NCBI36
NG_008481.4:g.50447_50449del , LRG_130:g.50447_50449del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.-19+42_-19+44del	ENSP00000473355.2:n.-19+42_-19+44del
ENST00000505084.2:n.38+42_38+44del
ENST00000505350.2:c.166-16906_166-16904del	ENSP00000481752.1:n.166-16906_166-16904del
ENST00000507379.6:c.166-28359_166-28357del	ENSP00000423224.2:n.166-28359_166-28357del
ENST00000509732.6:c.-18-16906_-18-16904del	ENSP00000426541.2:n.-18-16906_-18-16904del
ENST00000257430.9:c.-19+42_-19+44del MANE Select	ENSP00000257430.4:n.-19+42_-19+44del
ENST00000257430.8:c.-19+42_-19+44del	ENSP00000257430.4:n.-19+42_-19+44del
ENST00000505350.1:c.166-16906_166-16904del	ENSP00000481752.1:n.166-16906_166-16904del
ENST00000507379.5:c.166-28359_166-28357del	ENSP00000423224.1:n.166-28359_166-28357del
ENST00000508376.6:c.-127+42_-127+44del	ENSP00000427089.2:n.-127+42_-127+44del
ENST00000508624.5:c.-19+42_-19+44del	ENSP00000424265.1:n.-19+42_-19+44del
ENST00000509732.5:c.-18-16906_-18-16904del	ENSP00000426541.1:n.-18-16906_-18-16904del
NM_000038.5:c.-19+42_-19+44del	NP_000029.2:n.-19+42_-19+44del
NM_001127510.2:c.-127+42_-127+44del	NP_001120982.1:n.-127+42_-127+44del
NM_001127511.2:c.166-28359_166-28357del	NP_001120983.2:n.166-28359_166-28357del
NM_001354895.1:c.-18-16906_-18-16904del	NP_001341824.1:n.-18-16906_-18-16904del
NM_001354896.1:c.-19+42_-19+44del	NP_001341825.1:n.-19+42_-19+44del
NM_001354897.1:c.166-28359_166-28357del	NP_001341826.1:n.166-28359_166-28357del
NM_001354898.1:c.-49+42_-49+44del	NP_001341827.1:n.-49+42_-49+44del
NM_001354899.1:c.-19+42_-19+44del	NP_001341828.1:n.-19+42_-19+44del
NM_001354900.1:c.-43+42_-43+44del	NP_001341829.1:n.-43+42_-43+44del
NM_001354901.1:c.-43+42_-43+44del	NP_001341830.1:n.-43+42_-43+44del
NM_001354902.1:c.166-28359_166-28357del	NP_001341831.1:n.166-28359_166-28357del
NM_001354903.1:c.-19+42_-19+44del	NP_001341832.1:n.-19+42_-19+44del
NM_001354904.1:c.-49+42_-49+44del	NP_001341833.1:n.-49+42_-49+44del
NM_001354905.1:c.-43+42_-43+44del	NP_001341834.1:n.-43+42_-43+44del
NM_001354906.1:c.-1054+42_-1054+44del	NP_001341835.1:n.-1054+42_-1054+44del
NM_000038.6:c.-19+42_-19+44del MANE Select	NP_000029.2:n.-19+42_-19+44del
NM_001127510.3:c.-127+42_-127+44del	NP_001120982.1:n.-127+42_-127+44del
NM_001127511.3:c.166-28359_166-28357del	NP_001120983.2:n.166-28359_166-28357del
NM_001354895.2:c.-18-16906_-18-16904del	NP_001341824.1:n.-18-16906_-18-16904del
NM_001354896.2:c.-19+42_-19+44del	NP_001341825.1:n.-19+42_-19+44del
NM_001354897.2:c.166-28359_166-28357del	NP_001341826.1:n.166-28359_166-28357del
NM_001354898.2:c.-49+42_-49+44del	NP_001341827.1:n.-49+42_-49+44del
NM_001354899.2:c.-19+42_-19+44del	NP_001341828.1:n.-19+42_-19+44del
NM_001354900.2:c.-43+42_-43+44del	NP_001341829.1:n.-43+42_-43+44del
NM_001354901.2:c.-43+42_-43+44del	NP_001341830.1:n.-43+42_-43+44del
NM_001354902.2:c.166-28359_166-28357del	NP_001341831.1:n.166-28359_166-28357del
NM_001354903.2:c.-19+42_-19+44del	NP_001341832.1:n.-19+42_-19+44del
NM_001354904.2:c.-49+42_-49+44del	NP_001341833.1:n.-49+42_-49+44del
NM_001354905.2:c.-43+42_-43+44del	NP_001341834.1:n.-43+42_-43+44del
NM_001354906.2:c.-1054+42_-1054+44del	NP_001341835.1:n.-1054+42_-1054+44del