Canonical Allele Identifier: CA124925034
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 645010
ClinVar RCV Id: RCV003653340
dbSNP Id: rs561513597

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707610C>A , CM000667.2:g.112707610C>A GRCh38
NC_000005.9:g.112043307C>A , CM000667.1:g.112043307C>A GRCh37
NC_000005.8:g.112071206C>A NCBI36
NG_008481.4:g.20090C>A , LRG_130:g.20090C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.-108C>A ENSP00000481752.1:n.-108C>A
ENST00000507379.6:c.-108C>A ENSP00000423224.2:n.-108C>A
ENST00000509732.6:c.-58C>A ENSP00000426541.2:n.-58C>A
ENST00000505350.1:c.-108C>A ENSP00000481752.1:n.-108C>A
ENST00000507379.5:c.-108C>A ENSP00000423224.1:n.-108C>A
ENST00000509732.5:c.-58C>A ENSP00000426541.1:n.-58C>A
NM_001127511.2:c.-108C>A NP_001120983.2:n.-108C>A
NM_001354895.1:c.-291C>A NP_001341824.1:n.-291C>A
NM_001354897.1:c.-108C>A NP_001341826.1:n.-108C>A
NM_001354902.1:c.-108C>A NP_001341831.1:n.-108C>A
NM_001127511.3:c.-108C>A NP_001120983.2:n.-108C>A
NM_001354895.2:c.-291C>A NP_001341824.1:n.-291C>A
NM_001354897.2:c.-108C>A NP_001341826.1:n.-108C>A
NM_001354902.2:c.-108C>A NP_001341831.1:n.-108C>A