Canonical Allele Identifier: CA2697546388

Gene: APC

Linked Data

• ClinVar Variation Id: 2700026
• ClinVar RCV Id: RCV003536215

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707613_112707614delinsTT , CM000667.2:g.112707613_112707614delinsTT	GRCh38
NC_000005.9:g.112043310_112043311delinsTT , CM000667.1:g.112043310_112043311delinsTT	GRCh37
NC_000005.8:g.112071209_112071210delinsTT	NCBI36
NG_008481.4:g.20093_20094delinsTT , LRG_130:g.20093_20094delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-105_-104delinsTT	ENSP00000481752.1:n.-105_-104delinsTT
ENST00000507379.6:c.-105_-104delinsTT	ENSP00000423224.2:n.-105_-104delinsTT
ENST00000509732.6:c.-55_-54delinsTT	ENSP00000426541.2:n.-55_-54delinsTT
ENST00000505350.1:c.-105_-104delinsTT	ENSP00000481752.1:n.-105_-104delinsTT
ENST00000507379.5:c.-105_-104delinsTT	ENSP00000423224.1:n.-105_-104delinsTT
ENST00000509732.5:c.-55_-54delinsTT	ENSP00000426541.1:n.-55_-54delinsTT
NM_001127511.2:c.-105_-104delinsTT	NP_001120983.2:n.-105_-104delinsTT
NM_001354895.1:c.-288_-287delinsTT	NP_001341824.1:n.-288_-287delinsTT
NM_001354897.1:c.-105_-104delinsTT	NP_001341826.1:n.-105_-104delinsTT
NM_001354902.1:c.-105_-104delinsTT	NP_001341831.1:n.-105_-104delinsTT
NM_001127511.3:c.-105_-104delinsTT	NP_001120983.2:n.-105_-104delinsTT
NM_001354895.2:c.-288_-287delinsTT	NP_001341824.1:n.-288_-287delinsTT
NM_001354897.2:c.-105_-104delinsTT	NP_001341826.1:n.-105_-104delinsTT
NM_001354902.2:c.-105_-104delinsTT	NP_001341831.1:n.-105_-104delinsTT