Canonical Allele Identifier: CA006071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82801
ClinVar RCV Id: RCV000073790
dbSNP Id: rs11954856

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112751630T>G , CM000667.2:g.112751630T>G GRCh38
NC_000005.9:g.112087327T>G , CM000667.1:g.112087327T>G GRCh37
NC_000005.8:g.112115226T>G NCBI36
NG_008481.4:g.64110T>G , LRG_130:g.64110T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000257430.9:c.-18-3243T>G MANE Select ENSP00000257430.4:n.-18-3243T>G
ENST00000257430.8:c.-18-3243T>G ENSP00000257430.4:n.-18-3243T>G
ENST00000505350.1:c.166-3243T>G ENSP00000481752.1:n.166-3243T>G
ENST00000507379.5:c.166-14696T>G ENSP00000423224.1:n.166-14696T>G
ENST00000508376.6:c.-18-3243T>G ENSP00000427089.2:n.-18-3243T>G
ENST00000508624.5:c.-18-3243T>G ENSP00000424265.1:n.-18-3243T>G
ENST00000509732.5:c.-18-3243T>G ENSP00000426541.1:n.-18-3243T>G
ENST00000512211.6:c.-18-3243T>G ENSP00000423828.2:n.-18-3243T>G
NM_000038.5:c.-18-3243T>G NP_000029.2:n.-18-3243T>G
NM_001127510.2:c.-18-3243T>G NP_001120982.1:n.-18-3243T>G
NM_001127511.2:c.166-14696T>G NP_001120983.2:n.166-14696T>G
NM_001354895.1:c.-18-3243T>G NP_001341824.1:n.-18-3243T>G
NM_001354896.1:c.-18-3243T>G NP_001341825.1:n.-18-3243T>G
NM_001354897.1:c.166-14696T>G NP_001341826.1:n.166-14696T>G
NM_001354898.1:c.60+13170T>G NP_001341827.1:n.60+13170T>G
NM_001354899.1:c.-18-3243T>G NP_001341828.1:n.-18-3243T>G
NM_001354900.1:c.-43+13705T>G NP_001341829.1:n.-43+13705T>G
NM_001354901.1:c.-43+13705T>G NP_001341830.1:n.-43+13705T>G
NM_001354902.1:c.166-14696T>G NP_001341831.1:n.166-14696T>G
NM_001354903.1:c.-18-3243T>G NP_001341832.1:n.-18-3243T>G
NM_001354904.1:c.60+13170T>G NP_001341833.1:n.60+13170T>G
NM_001354905.1:c.-43+13705T>G NP_001341834.1:n.-43+13705T>G
NM_001354906.1:c.-1053-3243T>G NP_001341835.1:n.-1053-3243T>G
NM_000038.6:c.-18-3243T>G MANE Select NP_000029.2:n.-18-3243T>G
NM_001127510.3:c.-18-3243T>G NP_001120982.1:n.-18-3243T>G
NM_001127511.3:c.166-14696T>G NP_001120983.2:n.166-14696T>G
NM_001354895.2:c.-18-3243T>G NP_001341824.1:n.-18-3243T>G
NM_001354896.2:c.-18-3243T>G NP_001341825.1:n.-18-3243T>G
NM_001354897.2:c.166-14696T>G NP_001341826.1:n.166-14696T>G
NM_001354898.2:c.60+13170T>G NP_001341827.1:n.60+13170T>G
NM_001354899.2:c.-18-3243T>G NP_001341828.1:n.-18-3243T>G
NM_001354900.2:c.-43+13705T>G NP_001341829.1:n.-43+13705T>G
NM_001354901.2:c.-43+13705T>G NP_001341830.1:n.-43+13705T>G
NM_001354902.2:c.166-14696T>G NP_001341831.1:n.166-14696T>G
NM_001354903.2:c.-18-3243T>G NP_001341832.1:n.-18-3243T>G
NM_001354904.2:c.60+13170T>G NP_001341833.1:n.60+13170T>G
NM_001354905.2:c.-43+13705T>G NP_001341834.1:n.-43+13705T>G
NM_001354906.2:c.-1053-3243T>G NP_001341835.1:n.-1053-3243T>G