Canonical Allele Identifier: CA2767950550
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707829_112707844del , CM000667.2:g.112707829_112707844del GRCh38
NC_000005.9:g.112043526_112043541del , CM000667.1:g.112043526_112043541del GRCh37
NC_000005.8:g.112071425_112071440del NCBI36
NG_008481.4:g.20309_20324del , LRG_130:g.20309_20324del

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.112_127del ENSP00000481752.1:p.Thr38AlafsTer29
ENST00000507379.6:c.112_127del ENSP00000423224.2:p.Thr38AlafsTer?
ENST00000509732.6:c.-19+180_-19+195del ENSP00000426541.2:n.-19+180_-19+195del
ENST00000505350.1:c.112_127del ENSP00000481752.1:p.Thr38AlafsTer29
ENST00000507379.5:c.112_127del ENSP00000423224.1:p.Thr38AlafsTer?
ENST00000509732.5:c.-19+180_-19+195del ENSP00000426541.1:n.-19+180_-19+195del
NM_001127511.2:c.112_127del NP_001120983.2:p.Thr38AlafsTer?
NM_001354895.1:c.-72_-57del NP_001341824.1:n.-72_-57del
NM_001354897.1:c.112_127del NP_001341826.1:p.Thr38AlafsTer?
NM_001354902.1:c.112_127del NP_001341831.1:p.Thr38AlafsTer?
NM_001127511.3:c.112_127del NP_001120983.2:p.Thr38AlafsTer?
NM_001354895.2:c.-72_-57del NP_001341824.1:n.-72_-57del
NM_001354897.2:c.112_127del NP_001341826.1:p.Thr38AlafsTer?
NM_001354902.2:c.112_127del NP_001341831.1:p.Thr38AlafsTer?