Canonical Allele Identifier: CA2580072286

Gene: APC

Linked Data

• ClinVar Variation Id: 2133909
• ClinVar RCV Id: RCV003745538

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707584_112707585insGCGCTGCT , CM000667.2:g.112707584_112707585insGCGCTGCT	GRCh38
NC_000005.9:g.112043281_112043282insGCGCTGCT , CM000667.1:g.112043281_112043282insGCGCTGCT	GRCh37
NC_000005.8:g.112071180_112071181insGCGCTGCT	NCBI36
NG_008481.4:g.20064_20065insGCGCTGCT , LRG_130:g.20064_20065insGCGCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-134_-133insGCGCTGCT	ENSP00000481752.1:n.-134_-133insGCGCTGCT
ENST00000507379.6:c.-134_-133insGCGCTGCT	ENSP00000423224.2:n.-134_-133insGCGCTGCT
ENST00000509732.6:c.-84_-83insGCGCTGCT	ENSP00000426541.2:n.-84_-83insGCGCTGCT
ENST00000505350.1:c.-134_-133insGCGCTGCT	ENSP00000481752.1:n.-134_-133insGCGCTGCT
ENST00000507379.5:c.-134_-133insGCGCTGCT	ENSP00000423224.1:n.-134_-133insGCGCTGCT
ENST00000509732.5:c.-84_-83insGCGCTGCT	ENSP00000426541.1:n.-84_-83insGCGCTGCT
NM_001127511.2:c.-134_-133insGCGCTGCT	NP_001120983.2:n.-134_-133insGCGCTGCT
NM_001354895.1:c.-317_-316insGCGCTGCT	NP_001341824.1:n.-317_-316insGCGCTGCT
NM_001354897.1:c.-134_-133insGCGCTGCT	NP_001341826.1:n.-134_-133insGCGCTGCT
NM_001354902.1:c.-134_-133insGCGCTGCT	NP_001341831.1:n.-134_-133insGCGCTGCT
NM_001127511.3:c.-134_-133insGCGCTGCT	NP_001120983.2:n.-134_-133insGCGCTGCT
NM_001354895.2:c.-317_-316insGCGCTGCT	NP_001341824.1:n.-317_-316insGCGCTGCT
NM_001354897.2:c.-134_-133insGCGCTGCT	NP_001341826.1:n.-134_-133insGCGCTGCT
NM_001354902.2:c.-134_-133insGCGCTGCT	NP_001341831.1:n.-134_-133insGCGCTGCT