Canonical Allele Identifier: CA2767951390
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112737847_112737848del , CM000667.2:g.112737847_112737848del GRCh38
NC_000005.9:g.112073544_112073545del , CM000667.1:g.112073544_112073545del GRCh37
NC_000005.8:g.112101443_112101444del NCBI36
NG_008481.4:g.50327_50328del , LRG_130:g.50327_50328del

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.166-17026_166-17025del ENSP00000481752.1:n.166-17026_166-17025del
ENST00000507379.6:c.166-28479_166-28478del ENSP00000423224.2:n.166-28479_166-28478del
ENST00000509732.6:c.-18-17026_-18-17025del ENSP00000426541.2:n.-18-17026_-18-17025del
ENST00000505350.1:c.166-17026_166-17025del ENSP00000481752.1:n.166-17026_166-17025del
ENST00000507379.5:c.166-28479_166-28478del ENSP00000423224.1:n.166-28479_166-28478del
ENST00000509732.5:c.-18-17026_-18-17025del ENSP00000426541.1:n.-18-17026_-18-17025del
NM_001127511.2:c.166-28479_166-28478del NP_001120983.2:n.166-28479_166-28478del
NM_001354895.1:c.-18-17026_-18-17025del NP_001341824.1:n.-18-17026_-18-17025del
NM_001354897.1:c.166-28479_166-28478del NP_001341826.1:n.166-28479_166-28478del
NM_001354902.1:c.166-28479_166-28478del NP_001341831.1:n.166-28479_166-28478del
NM_001127511.3:c.166-28479_166-28478del NP_001120983.2:n.166-28479_166-28478del
NM_001354895.2:c.-18-17026_-18-17025del NP_001341824.1:n.-18-17026_-18-17025del
NM_001354897.2:c.166-28479_166-28478del NP_001341826.1:n.166-28479_166-28478del
NM_001354902.2:c.166-28479_166-28478del NP_001341831.1:n.166-28479_166-28478del