Canonical Allele Identifier: CA1139770842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1766545

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112815591_112815595delinsCA , CM000667.2:g.112815591_112815595delinsCA GRCh38
NC_000005.9:g.112151288_112151292delinsCA , CM000667.1:g.112151288_112151292delinsCA GRCh37
NC_000005.8:g.112179187_112179191delinsCA NCBI36
NG_008481.4:g.128071_128075delinsCA , LRG_130:g.128071_128075delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.931_933+2delinsCA
ENST00000504915.3:c.931_933+2delinsCA
ENST00000505084.2:n.987_989+2delinsCA
ENST00000505350.2:c.*937_*939+2delinsCA
ENST00000507379.6:c.877_879+2delinsCA
ENST00000509732.6:c.931_933+2delinsCA
ENST00000512211.7:c.931_933+2delinsCA
ENST00000257430.9:c.931_933+2delinsCA
ENST00000257430.8:c.931_933+2delinsCA
ENST00000507379.5:c.877_879+2delinsCA
ENST00000508376.6:c.931_933+2delinsCA
ENST00000508624.5:c.*253_*255+2delinsCA
ENST00000512211.6:c.931_933+2delinsCA
NM_000038.5:c.931_933+2delinsCA
NM_001127510.2:c.931_933+2delinsCA
NM_001127511.2:c.877_879+2delinsCA
NM_001354895.1:c.931_933+2delinsCA
NM_001354896.1:c.931_933+2delinsCA
NM_001354897.1:c.961_963+2delinsCA
NM_001354898.1:c.856_858+2delinsCA
NM_001354899.1:c.847_849+2delinsCA
NM_001354900.1:c.754_756+2delinsCA
NM_001354901.1:c.754_756+2delinsCA
NM_001354902.1:c.961_963+2delinsCA
NM_001354903.1:c.931_933+2delinsCA
NM_001354904.1:c.856_858+2delinsCA
NM_001354905.1:c.754_756+2delinsCA
NM_001354906.1:c.82_84+2delinsCA
NM_000038.6:c.931_933+2delinsCA
NM_001127510.3:c.931_933+2delinsCA
NM_001127511.3:c.877_879+2delinsCA
NM_001354895.2:c.931_933+2delinsCA
NM_001354896.2:c.931_933+2delinsCA
NM_001354897.2:c.961_963+2delinsCA
NM_001354898.2:c.856_858+2delinsCA
NM_001354899.2:c.847_849+2delinsCA
NM_001354900.2:c.754_756+2delinsCA
NM_001354901.2:c.754_756+2delinsCA
NM_001354902.2:c.961_963+2delinsCA
NM_001354903.2:c.931_933+2delinsCA
NM_001354904.2:c.856_858+2delinsCA
NM_001354905.2:c.754_756+2delinsCA
NM_001354906.2:c.82_84+2delinsCA