Linked Data
dbSNP Id:
rs776224675
MyVariant Identifiers:
chr12:g.110777064_110777065insGCCAC (hg19)
chr12:g.110339259_110339260insGCCAC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110339259_110339260insGCCAC , CM000674.2:g.110339259_110339260insGCCAC | GRCh38 |
| NC_000012.11:g.110777064_110777065insGCCAC , CM000674.1:g.110777064_110777065insGCCAC | GRCh37 |
| NC_000012.10:g.109261447_109261448insGCCAC | NCBI36 |
| NG_007097.2:g.62633_62634insGCCAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539276.7:c.1420-22_1420-21insGCCAC MANE Select | ENSP00000440045.2:n.1420-22_1420-21insGCCAC | |
| ENST00000308664.10:c.1420-22_1420-21insGCCAC | ENSP00000311186.6:n.1420-22_1420-21insGCCAC | |
| ENST00000377685.9:c.*1260-22_*1260-21insGCCAC | ENSP00000366913.4:n.*1260-22_*1260-21insGCCAC | |
| ENST00000539276.6:c.1420-22_1420-21insGCCAC | ENSP00000440045.2:n.1420-22_1420-21insGCCAC | |
| ENST00000548169.2:c.1091-22_1091-21insGCCAC | ||
| NM_001681.3:c.1420-22_1420-21insGCCAC | NP_001672.1:n.1420-22_1420-21insGCCAC | |
| NM_170665.3:c.1420-22_1420-21insGCCAC | NP_733765.1:n.1420-22_1420-21insGCCAC | |
| XM_005253888.1:c.1420-22_1420-21insGCCAC | XP_005253945.1:n.1420-22_1420-21insGCCAC | |
| XM_011538402.1:c.1420-22_1420-21insGCCAC | XP_011536704.1:n.1420-22_1420-21insGCCAC | |
| XM_011538403.1:c.1420-22_1420-21insGCCAC | XP_011536705.1:n.1420-22_1420-21insGCCAC | |
| XR_243009.1:n.1426-22_1426-21insGCCAC | ||
| XM_005253888.3:c.1420-22_1420-21insGCCAC | XP_005253945.1:n.1420-22_1420-21insGCCAC | |
| XM_011538402.3:c.1420-22_1420-21insGCCAC | XP_011536704.1:n.1420-22_1420-21insGCCAC | |
| XR_002957329.1:n.1426-22_1426-21insGCCAC | ||
| XR_243009.3:n.1426-22_1426-21insGCCAC | ||
| NM_170665.4:c.1420-22_1420-21insGCCAC MANE Select | NP_733765.1:n.1420-22_1420-21insGCCAC | |
| NM_001681.4:c.1420-22_1420-21insGCCAC | NP_001672.1:n.1420-22_1420-21insGCCAC |