Canonical Allele Identifier: CA2767951382
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112737845_112737846insAAGT , CM000667.2:g.112737845_112737846insAAGT GRCh38
NC_000005.9:g.112073542_112073543insAAGT , CM000667.1:g.112073542_112073543insAAGT GRCh37
NC_000005.8:g.112101441_112101442insAAGT NCBI36
NG_008481.4:g.50325_50326insAAGT , LRG_130:g.50325_50326insAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.166-17028_166-17027insAAGT ENSP00000481752.1:n.166-17028_166-17027insAAGT
ENST00000507379.6:c.166-28481_166-28480insAAGT ENSP00000423224.2:n.166-28481_166-28480insAAGT
ENST00000509732.6:c.-18-17028_-18-17027insAAGT ENSP00000426541.2:n.-18-17028_-18-17027insAAGT
ENST00000505350.1:c.166-17028_166-17027insAAGT ENSP00000481752.1:n.166-17028_166-17027insAAGT
ENST00000507379.5:c.166-28481_166-28480insAAGT ENSP00000423224.1:n.166-28481_166-28480insAAGT
ENST00000509732.5:c.-18-17028_-18-17027insAAGT ENSP00000426541.1:n.-18-17028_-18-17027insAAGT
NM_001127511.2:c.166-28481_166-28480insAAGT NP_001120983.2:n.166-28481_166-28480insAAGT
NM_001354895.1:c.-18-17028_-18-17027insAAGT NP_001341824.1:n.-18-17028_-18-17027insAAGT
NM_001354897.1:c.166-28481_166-28480insAAGT NP_001341826.1:n.166-28481_166-28480insAAGT
NM_001354902.1:c.166-28481_166-28480insAAGT NP_001341831.1:n.166-28481_166-28480insAAGT
NM_001127511.3:c.166-28481_166-28480insAAGT NP_001120983.2:n.166-28481_166-28480insAAGT
NM_001354895.2:c.-18-17028_-18-17027insAAGT NP_001341824.1:n.-18-17028_-18-17027insAAGT
NM_001354897.2:c.166-28481_166-28480insAAGT NP_001341826.1:n.166-28481_166-28480insAAGT
NM_001354902.2:c.166-28481_166-28480insAAGT NP_001341831.1:n.166-28481_166-28480insAAGT