Linked Data
ClinVar Variation Id:
82927
ClinVar RCV Id:
RCV000073916
dbSNP Id:
rs414098
gnomAD v2:
5-112113772-G-A
gnomAD v3:
5-112778075-G-A
gnomAD v4:
5-112778075-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112778075G>A , CM000667.2:g.112778075G>A | GRCh38 |
| NC_000005.9:g.112113772G>A , CM000667.1:g.112113772G>A | GRCh37 |
| NC_000005.8:g.112141671G>A | NCBI36 |
| NG_008481.4:g.90555G>A , LRG_130:g.90555G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000502371.3:c.531+2338G>A (APC) | ENSP00000484935.2:n.531+2338G>A | |
| ENST00000504915.3:c.531+2338G>A (APC) | ENSP00000473355.2:n.531+2338G>A | |
| ENST00000505084.2:n.587+2338G>A (APC) | ||
| ENST00000505350.2:c.*537+2338G>A (APC) | ENSP00000481752.1:n.*537+2338G>A | |
| ENST00000507379.6:c.561+2338G>A (APC) | ENSP00000423224.2:n.561+2338G>A | |
| ENST00000509732.6:c.531+2338G>A (APC) | ENSP00000426541.2:n.531+2338G>A | |
| ENST00000512211.7:c.531+2338G>A (APC) | ENSP00000423828.3:n.531+2338G>A | |
| ENST00000257430.9:c.531+2338G>A (APC) MANE Select | ENSP00000257430.4:n.531+2338G>A | |
| ENST00000257430.8:c.531+2338G>A (APC) | ENSP00000257430.4:n.531+2338G>A | |
| ENST00000507379.5:c.561+2338G>A (APC) | ENSP00000423224.1:n.561+2338G>A | |
| ENST00000508108.2:n.87C>T (CBX3P3) | ||
| ENST00000508376.6:c.531+2338G>A (APC) | ENSP00000427089.2:n.531+2338G>A | |
| ENST00000508624.5:c.531+2338G>A (APC) | ENSP00000424265.1:n.531+2338G>A | |
| ENST00000512211.6:c.531+2338G>A (APC) | ENSP00000423828.2:n.531+2338G>A | |
| NM_000038.5:c.531+2338G>A (APC) | NP_000029.2:n.531+2338G>A | |
| NM_001127510.2:c.531+2338G>A (APC) | NP_001120982.1:n.531+2338G>A | |
| NM_001127511.2:c.561+2338G>A (APC) | NP_001120983.2:n.561+2338G>A | |
| NM_001354895.1:c.531+2338G>A (APC) | NP_001341824.1:n.531+2338G>A | |
| NM_001354896.1:c.531+2338G>A (APC) | NP_001341825.1:n.531+2338G>A | |
| NM_001354897.1:c.561+2338G>A (APC) | NP_001341826.1:n.561+2338G>A | |
| NM_001354898.1:c.456+2338G>A (APC) | NP_001341827.1:n.456+2338G>A | |
| NM_001354899.1:c.531+2338G>A (APC) | NP_001341828.1:n.531+2338G>A | |
| NM_001354900.1:c.354+2338G>A (APC) | NP_001341829.1:n.354+2338G>A | |
| NM_001354901.1:c.354+2338G>A (APC) | NP_001341830.1:n.354+2338G>A | |
| NM_001354902.1:c.561+2338G>A (APC) | NP_001341831.1:n.561+2338G>A | |
| NM_001354903.1:c.531+2338G>A (APC) | NP_001341832.1:n.531+2338G>A | |
| NM_001354904.1:c.456+2338G>A (APC) | NP_001341833.1:n.456+2338G>A | |
| NM_001354905.1:c.354+2338G>A (APC) | NP_001341834.1:n.354+2338G>A | |
| NM_001354906.1:c.-505+2338G>A (APC) | NP_001341835.1:n.-505+2338G>A | |
| NM_000038.6:c.531+2338G>A (APC) MANE Select | NP_000029.2:n.531+2338G>A | |
| NM_001127510.3:c.531+2338G>A (APC) | NP_001120982.1:n.531+2338G>A | |
| NM_001127511.3:c.561+2338G>A (APC) | NP_001120983.2:n.561+2338G>A | |
| NM_001354895.2:c.531+2338G>A (APC) | NP_001341824.1:n.531+2338G>A | |
| NM_001354896.2:c.531+2338G>A (APC) | NP_001341825.1:n.531+2338G>A | |
| NM_001354897.2:c.561+2338G>A (APC) | NP_001341826.1:n.561+2338G>A | |
| NM_001354898.2:c.456+2338G>A (APC) | NP_001341827.1:n.456+2338G>A | |
| NM_001354899.2:c.531+2338G>A (APC) | NP_001341828.1:n.531+2338G>A | |
| NM_001354900.2:c.354+2338G>A (APC) | NP_001341829.1:n.354+2338G>A | |
| NM_001354901.2:c.354+2338G>A (APC) | NP_001341830.1:n.354+2338G>A | |
| NM_001354902.2:c.561+2338G>A (APC) | NP_001341831.1:n.561+2338G>A | |
| NM_001354903.2:c.531+2338G>A (APC) | NP_001341832.1:n.531+2338G>A | |
| NM_001354904.2:c.456+2338G>A (APC) | NP_001341833.1:n.456+2338G>A | |
| NM_001354905.2:c.354+2338G>A (APC) | NP_001341834.1:n.354+2338G>A | |
| NM_001354906.2:c.-505+2338G>A (APC) | NP_001341835.1:n.-505+2338G>A |