Linked Data
gnomAD v4:
4-186191641-T-TTCCCACCCTCCGATCAGCCA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186191641_186191642insTCCCACCCTCCGATCAGCCA , CM000666.2:g.186191641_186191642insTCCCACCCTCCGATCAGCCA | GRCh38 |
| NC_000004.11:g.187112795_187112796insTCCCACCCTCCGATCAGCCA , CM000666.1:g.187112795_187112796insTCCCACCCTCCGATCAGCCA | GRCh37 |
| NC_000004.10:g.187349789_187349790insTCCCACCCTCCGATCAGCCA | NCBI36 |
| NG_007965.1:g.5122_5123insTCCCACCCTCCGATCAGCCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.-183_-182insTCCCACCCTCCGATCAGCCA MANE Select | ENSP00000368079.4:n.-183_-182insTCCCACCCTCCGATCAGCCA | |
| ENST00000378802.4:c.-183_-182insTCCCACCCTCCGATCAGCCA | ENSP00000368079.4:n.-183_-182insTCCCACCCTCCGATCAGCCA | |
| NM_207352.3:c.-183_-182insTCCCACCCTCCGATCAGCCA | NP_997235.3:n.-183_-182insTCCCACCCTCCGATCAGCCA | |
| XM_005262935.2:c.-183_-182insTCCCACCCTCCGATCAGCCA | XP_005262992.1:n.-183_-182insTCCCACCCTCCGATCAGCCA | |
| NM_207352.4:c.-183_-182insTCCCACCCTCCGATCAGCCA MANE Select | NP_997235.3:n.-183_-182insTCCCACCCTCCGATCAGCCA |