Canonical Allele Identifier: CA023461
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82697
ClinVar RCV Id: RCV000073686
dbSNP Id: rs75168477

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112727927A>C , CM000667.2:g.112727927A>C GRCh38
NC_000005.9:g.112063624A>C , CM000667.1:g.112063624A>C GRCh37
NC_000005.8:g.112091523A>C NCBI36
NG_008481.4:g.40407A>C , LRG_130:g.40407A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000505350.1:c.165+20045A>C ENSP00000481752.1:n.165+20045A>C
ENST00000507379.5:c.165+20045A>C ENSP00000423224.1:n.165+20045A>C
ENST00000509732.5:c.-19+20278A>C ENSP00000426541.1:n.-19+20278A>C
NM_001127511.2:c.165+20045A>C NP_001120983.2:n.165+20045A>C
NM_001354895.1:c.-19+20045A>C NP_001341824.1:n.-19+20045A>C
NM_001354897.1:c.165+20045A>C NP_001341826.1:n.165+20045A>C
NM_001354902.1:c.165+20045A>C NP_001341831.1:n.165+20045A>C
NM_001127511.3:c.165+20045A>C NP_001120983.2:n.165+20045A>C
NM_001354895.2:c.-19+20045A>C NP_001341824.1:n.-19+20045A>C
NM_001354897.2:c.165+20045A>C NP_001341826.1:n.165+20045A>C
NM_001354902.2:c.165+20045A>C NP_001341831.1:n.165+20045A>C