Canonical Allele Identifier: CA1573458487
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112737638_112737639delinsTG , CM000667.2:g.112737638_112737639delinsTG GRCh38
NC_000005.9:g.112073335_112073336delinsTG , CM000667.1:g.112073335_112073336delinsTG GRCh37
NC_000005.8:g.112101234_112101235delinsTG NCBI36
NG_008481.4:g.50118_50119delinsTG , LRG_130:g.50118_50119delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.166-17235_166-17234delinsTG ENSP00000481752.1:n.166-17235_166-17234delinsTG
ENST00000507379.6:c.166-28688_166-28687delinsTG ENSP00000423224.2:n.166-28688_166-28687delinsTG
ENST00000509732.6:c.-18-17235_-18-17234delinsTG ENSP00000426541.2:n.-18-17235_-18-17234delinsTG
ENST00000505350.1:c.166-17235_166-17234delinsTG ENSP00000481752.1:n.166-17235_166-17234delinsTG
ENST00000507379.5:c.166-28688_166-28687delinsTG ENSP00000423224.1:n.166-28688_166-28687delinsTG
ENST00000509732.5:c.-18-17235_-18-17234delinsTG ENSP00000426541.1:n.-18-17235_-18-17234delinsTG
NM_001127511.2:c.166-28688_166-28687delinsTG NP_001120983.2:n.166-28688_166-28687delinsTG
NM_001354895.1:c.-18-17235_-18-17234delinsTG NP_001341824.1:n.-18-17235_-18-17234delinsTG
NM_001354897.1:c.166-28688_166-28687delinsTG NP_001341826.1:n.166-28688_166-28687delinsTG
NM_001354902.1:c.166-28688_166-28687delinsTG NP_001341831.1:n.166-28688_166-28687delinsTG
NM_001127511.3:c.166-28688_166-28687delinsTG NP_001120983.2:n.166-28688_166-28687delinsTG
NM_001354895.2:c.-18-17235_-18-17234delinsTG NP_001341824.1:n.-18-17235_-18-17234delinsTG
NM_001354897.2:c.166-28688_166-28687delinsTG NP_001341826.1:n.166-28688_166-28687delinsTG
NM_001354902.2:c.166-28688_166-28687delinsTG NP_001341831.1:n.166-28688_166-28687delinsTG