Linked Data
ClinVar Variation Id:
166692
dbSNP Id:
rs786200965
MyVariant Identifiers:
chr22:g.51065685_51065690delinsCCCAAGGTT (hg19)
chr22:g.50627257_50627262delinsCCCAAGGTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50627257_50627262delinsCCCAAGGTT , CM000684.2:g.50627257_50627262delinsCCCAAGGTT | GRCh38 |
| NC_000022.10:g.51065685_51065690delinsCCCAAGGTT , CM000684.1:g.51065685_51065690delinsCCCAAGGTT | GRCh37 |
| NC_000022.9:g.49412551_49412556delinsCCCAAGGTT | NCBI36 |
| NG_009260.2:g.5918_5923delinsAACCTTGGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216124.10:c.369_374delinsAACCTTGGG MANE Select | ENSP00000216124.5:p.Gly124_Lys125delinsThrLeuGly | |
| ENST00000216124.9:c.369_374delinsAACCTTGGG | ENSP00000216124.5:p.Gly124_Lys125delinsThrLeuGly | |
| ENST00000356098.9:c.369_374delinsAACCTTGGG | ENSP00000348406.5:p.Gly124_Lys125delinsThrLeuGly | |
| ENST00000395619.3:c.369_374delinsAACCTTGGG | ENSP00000378981.3:p.Gly124_Lys125delinsThrLeuGly | |
| ENST00000395621.7:c.369_374delinsAACCTTGGG | ENSP00000378983.3:p.Gly124_Lys125delinsThrLeuGly | |
| ENST00000453344.6:c.111_116delinsAACCTTGGG | ENSP00000412542.2:p.Gly38_Lys39delinsThrLeuGly | |
| ENST00000551731.1:n.760_765delinsAACCTTGGG | ||
| NM_000487.5:c.369_374delinsAACCTTGGG | NP_000478.3:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085425.2:c.369_374delinsAACCTTGGG | NP_001078894.2:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085426.2:c.369_374delinsAACCTTGGG | NP_001078895.2:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085427.2:c.369_374delinsAACCTTGGG | NP_001078896.2:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085428.2:c.111_116delinsAACCTTGGG | NP_001078897.1:p.Gly38_Lys39delinsThrLeuGly | |
| XM_011530690.1:c.111_116delinsAACCTTGGG | XP_011528992.1:p.Gly38_Lys39delinsThrLeuGly | |
| XM_011530691.1:c.369_374delinsAACCTTGGG | XP_011528993.1:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001362782.1:c.111_116delinsAACCTTGGG | NP_001349711.1:p.Gly38_Lys39delinsThrLeuGly | |
| XM_011530691.3:c.369_374delinsAACCTTGGG | XP_011528993.1:p.Gly124_Lys125delinsThrLeuGly | |
| XM_017028800.1:c.369_374delinsAACCTTGGG | XP_016884289.1:p.Gly124_Lys125delinsThrLeuGly | |
| XM_024452241.1:c.369_374delinsAACCTTGGG | XP_024308009.1:p.Gly124_Lys125delinsThrLeuGly | |
| NM_000487.6:c.369_374delinsAACCTTGGG MANE Select | NP_000478.3:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085425.3:c.369_374delinsAACCTTGGG | NP_001078894.2:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085426.3:c.369_374delinsAACCTTGGG | NP_001078895.2:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085427.3:c.369_374delinsAACCTTGGG | NP_001078896.2:p.Gly124_Lys125delinsThrLeuGly | |
| NM_001085428.3:c.111_116delinsAACCTTGGG | NP_001078897.1:p.Gly38_Lys39delinsThrLeuGly | |
| NM_001362782.2:c.111_116delinsAACCTTGGG | NP_001349711.1:p.Gly38_Lys39delinsThrLeuGly |