Linked Data
gnomAD v2:
6-116938698-C-CTTTTT
MyVariant Identifiers:
chr6:g.116938698_116938699insTTTTT (hg19)
chr6:g.116617535_116617536insTTTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.116617536_116617537insTTTTT , CM000668.2:g.116617536_116617537insTTTTT | GRCh38 |
| NC_000006.11:g.116938699_116938700insTTTTT , CM000668.1:g.116938699_116938700insTTTTT | GRCh37 |
| NC_000006.10:g.117045392_117045393insTTTTT | NCBI36 |
| NG_012934.1:g.6058_6059insTTTTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229554.10:c.686+227_686+228insTTTTT MANE Select | ENSP00000229554.5:n.686+227_686+228insTTTTT | |
| ENST00000229554.9:c.686+227_686+228insTTTTT | ENSP00000229554.5:n.686+227_686+228insTTTTT | |
| ENST00000368580.4:c.686+227_686+228insTTTTT | ENSP00000357569.4:n.686+227_686+228insTTTTT | |
| ENST00000368581.8:c.686+227_686+228insTTTTT | ENSP00000357570.4:n.686+227_686+228insTTTTT | |
| NM_001010892.2:c.686+227_686+228insTTTTT | NP_001010892.1:n.686+227_686+228insTTTTT | |
| NM_001161664.1:c.686+227_686+228insTTTTT | NP_001155136.1:n.686+227_686+228insTTTTT | |
| XM_006715469.2:c.686+227_686+228insTTTTT | XP_006715532.1:n.686+227_686+228insTTTTT | |
| XM_011535791.1:c.686+227_686+228insTTTTT | XP_011534093.1:n.686+227_686+228insTTTTT | |
| XM_011535792.1:c.686+227_686+228insTTTTT | XP_011534094.1:n.686+227_686+228insTTTTT | |
| XR_942416.1:n.3337+227_3337+228insTTTTT | ||
| XM_017010826.1:c.686+227_686+228insTTTTT | XP_016866315.1:n.686+227_686+228insTTTTT | |
| NM_001010892.3:c.686+227_686+228insTTTTT MANE Select | NP_001010892.1:n.686+227_686+228insTTTTT | |
| NM_001161664.2:c.686+227_686+228insTTTTT | NP_001155136.1:n.686+227_686+228insTTTTT |