Canonical Allele Identifier: CA015218
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82543
ClinVar RCV Id: RCV000073532
dbSNP Id: rs76601225

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112811070A>C , CM000667.2:g.112811070A>C GRCh38
NC_000005.9:g.112146767A>C , CM000667.1:g.112146767A>C GRCh37
NC_000005.8:g.112174666A>C NCBI36
NG_008481.4:g.123550A>C , LRG_130:g.123550A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.835-4425A>C ENSP00000484935.2:n.835-4425A>C
ENST00000504915.3:c.835-4425A>C ENSP00000473355.2:n.835-4425A>C
ENST00000505084.2:n.891-4425A>C
ENST00000505350.2:c.*841-4425A>C ENSP00000481752.1:n.*841-4425A>C
ENST00000507379.6:c.781-4425A>C ENSP00000423224.2:n.781-4425A>C
ENST00000509732.6:c.835-4425A>C ENSP00000426541.2:n.835-4425A>C
ENST00000512211.7:c.835-4425A>C ENSP00000423828.3:n.835-4425A>C
ENST00000257430.9:c.835-4425A>C MANE Select ENSP00000257430.4:n.835-4425A>C
ENST00000257430.8:c.835-4425A>C ENSP00000257430.4:n.835-4425A>C
ENST00000507379.5:c.781-4425A>C ENSP00000423224.1:n.781-4425A>C
ENST00000508376.6:c.835-4425A>C ENSP00000427089.2:n.835-4425A>C
ENST00000508624.5:c.*156+759A>C ENSP00000424265.1:n.*156+759A>C
ENST00000512211.6:c.835-4425A>C ENSP00000423828.2:n.835-4425A>C
NM_000038.5:c.835-4425A>C NP_000029.2:n.835-4425A>C
NM_001127510.2:c.835-4425A>C NP_001120982.1:n.835-4425A>C
NM_001127511.2:c.781-4425A>C NP_001120983.2:n.781-4425A>C
NM_001354895.1:c.835-4425A>C NP_001341824.1:n.835-4425A>C
NM_001354896.1:c.835-4425A>C NP_001341825.1:n.835-4425A>C
NM_001354897.1:c.865-4425A>C NP_001341826.1:n.865-4425A>C
NM_001354898.1:c.760-4425A>C NP_001341827.1:n.760-4425A>C
NM_001354899.1:c.751-4425A>C NP_001341828.1:n.751-4425A>C
NM_001354900.1:c.658-4425A>C NP_001341829.1:n.658-4425A>C
NM_001354901.1:c.658-4425A>C NP_001341830.1:n.658-4425A>C
NM_001354902.1:c.865-4425A>C NP_001341831.1:n.865-4425A>C
NM_001354903.1:c.835-4425A>C NP_001341832.1:n.835-4425A>C
NM_001354904.1:c.760-4425A>C NP_001341833.1:n.760-4425A>C
NM_001354905.1:c.658-4425A>C NP_001341834.1:n.658-4425A>C
NM_001354906.1:c.-16+759A>C NP_001341835.1:n.-16+759A>C
NM_000038.6:c.835-4425A>C MANE Select NP_000029.2:n.835-4425A>C
NM_001127510.3:c.835-4425A>C NP_001120982.1:n.835-4425A>C
NM_001127511.3:c.781-4425A>C NP_001120983.2:n.781-4425A>C
NM_001354895.2:c.835-4425A>C NP_001341824.1:n.835-4425A>C
NM_001354896.2:c.835-4425A>C NP_001341825.1:n.835-4425A>C
NM_001354897.2:c.865-4425A>C NP_001341826.1:n.865-4425A>C
NM_001354898.2:c.760-4425A>C NP_001341827.1:n.760-4425A>C
NM_001354899.2:c.751-4425A>C NP_001341828.1:n.751-4425A>C
NM_001354900.2:c.658-4425A>C NP_001341829.1:n.658-4425A>C
NM_001354901.2:c.658-4425A>C NP_001341830.1:n.658-4425A>C
NM_001354902.2:c.865-4425A>C NP_001341831.1:n.865-4425A>C
NM_001354903.2:c.835-4425A>C NP_001341832.1:n.835-4425A>C
NM_001354904.2:c.760-4425A>C NP_001341833.1:n.760-4425A>C
NM_001354905.2:c.658-4425A>C NP_001341834.1:n.658-4425A>C
NM_001354906.2:c.-16+759A>C NP_001341835.1:n.-16+759A>C