Canonical Allele Identifier: CA2739274984
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2775491
ClinVar RCV Id: RCV003745615

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707591_112707592delinsA , CM000667.2:g.112707591_112707592delinsA GRCh38
NC_000005.9:g.112043288_112043289delinsA , CM000667.1:g.112043288_112043289delinsA GRCh37
NC_000005.8:g.112071187_112071188delinsA NCBI36
NG_008481.4:g.20071_20072delinsA , LRG_130:g.20071_20072delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.-127_-126delinsA ENSP00000481752.1:n.-127_-126delinsA
ENST00000507379.6:c.-127_-126delinsA ENSP00000423224.2:n.-127_-126delinsA
ENST00000509732.6:c.-77_-76delinsA ENSP00000426541.2:n.-77_-76delinsA
ENST00000505350.1:c.-127_-126delinsA ENSP00000481752.1:n.-127_-126delinsA
ENST00000507379.5:c.-127_-126delinsA ENSP00000423224.1:n.-127_-126delinsA
ENST00000509732.5:c.-77_-76delinsA ENSP00000426541.1:n.-77_-76delinsA
NM_001127511.2:c.-127_-126delinsA NP_001120983.2:n.-127_-126delinsA
NM_001354895.1:c.-310_-309delinsA NP_001341824.1:n.-310_-309delinsA
NM_001354897.1:c.-127_-126delinsA NP_001341826.1:n.-127_-126delinsA
NM_001354902.1:c.-127_-126delinsA NP_001341831.1:n.-127_-126delinsA
NM_001127511.3:c.-127_-126delinsA NP_001120983.2:n.-127_-126delinsA
NM_001354895.2:c.-310_-309delinsA NP_001341824.1:n.-310_-309delinsA
NM_001354897.2:c.-127_-126delinsA NP_001341826.1:n.-127_-126delinsA
NM_001354902.2:c.-127_-126delinsA NP_001341831.1:n.-127_-126delinsA