Linked Data
gnomAD v2:
10-89717827-A-ATATCAGC
MyVariant Identifiers:
chr10:g.89717827_89717828insTATCAGC (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87958070_87958071insTATCAGC , CM000672.2:g.87958070_87958071insTATCAGC | GRCh38 |
| NC_000010.10:g.89717827_89717828insTATCAGC , CM000672.1:g.89717827_89717828insTATCAGC | GRCh37 |
| NC_000010.9:g.89707807_89707808insTATCAGC | NCBI36 |
| NG_007466.2:g.99632_99633insTATCAGC , LRG_311:g.99632_99633insTATCAGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.801+51_801+52insTATCAGC | ENSP00000514759.2:n.801+51_801+52insTATCAGC | |
| ENST00000710265.1:c.801+51_801+52insTATCAGC | ENSP00000518161.1:n.801+51_801+52insTATCAGC | |
| ENST00000472832.3:c.801+51_801+52insTATCAGC | ENSP00000483066.2:n.801+51_801+52insTATCAGC | |
| ENST00000688158.2:n.1536+51_1536+52insTATCAGC | ||
| ENST00000688922.2:c.*631+51_*631+52insTATCAGC | ENSP00000508742.2:n.*631+51_*631+52insTATCAGC | |
| ENST00000700021.1:c.756+51_756+52insTATCAGC | ENSP00000514757.1:n.756+51_756+52insTATCAGC | |
| ENST00000700022.1:c.*140+51_*140+52insTATCAGC | ENSP00000514758.1:n.*140+51_*140+52insTATCAGC | |
| ENST00000700023.1:n.1959+51_1959+52insTATCAGC | ||
| ENST00000700024.1:n.2193+51_2193+52insTATCAGC | ||
| ENST00000700025.1:n.1570+51_1570+52insTATCAGC | ||
| ENST00000700026.1:n.438+51_438+52insTATCAGC | ||
| ENST00000700029.1:c.635+51_635+52insTATCAGC | ||
| ENST00000706954.1:c.801+51_801+52insTATCAGC | ENSP00000516674.1:n.801+51_801+52insTATCAGC | |
| ENST00000706955.1:c.*836+51_*836+52insTATCAGC | ENSP00000516675.1:n.*836+51_*836+52insTATCAGC | |
| ENST00000686459.1:c.*387+51_*387+52insTATCAGC | ENSP00000508909.1:n.*387+51_*387+52insTATCAGC | |
| ENST00000688158.1:c.*912+51_*912+52insTATCAGC | ENSP00000509254.1:n.*912+51_*912+52insTATCAGC | |
| ENST00000688308.1:c.801+51_801+52insTATCAGC | ENSP00000508752.1:n.801+51_801+52insTATCAGC | |
| ENST00000688922.1:c.722+51_722+52insTATCAGC | ||
| ENST00000693560.1:c.1320+51_1320+52insTATCAGC | ENSP00000509861.1:n.1320+51_1320+52insTATCAGC | |
| ENST00000371953.8:c.801+51_801+52insTATCAGC MANE Select | ENSP00000361021.3:n.801+51_801+52insTATCAGC | |
| ENST00000371953.7:c.801+51_801+52insTATCAGC | ENSP00000361021.3:n.801+51_801+52insTATCAGC | |
| ENST00000472832.2:c.228+51_228+52insTATCAGC | ENSP00000483066.1:n.228+51_228+52insTATCAGC | |
| NM_000314.5:c.801+51_801+52insTATCAGC | NP_000305.3:n.801+51_801+52insTATCAGC | |
| NM_000314.6:c.801+51_801+52insTATCAGC | NP_000305.3:n.801+51_801+52insTATCAGC | |
| NM_001304717.2:c.1320+51_1320+52insTATCAGC | NP_001291646.2:n.1320+51_1320+52insTATCAGC | |
| NM_001304718.1:c.210+51_210+52insTATCAGC | NP_001291647.1:n.210+51_210+52insTATCAGC | |
| XM_006717926.2:c.756+51_756+52insTATCAGC | XP_006717989.1:n.756+51_756+52insTATCAGC | |
| XM_011539981.1:c.801+51_801+52insTATCAGC | XP_011538283.1:n.801+51_801+52insTATCAGC | |
| XM_011539982.1:c.705+51_705+52insTATCAGC | XP_011538284.1:n.705+51_705+52insTATCAGC | |
| XR_945791.1:n.1371+51_1371+52insTATCAGC | ||
| NM_000314.7:c.801+51_801+52insTATCAGC | NP_000305.3:n.801+51_801+52insTATCAGC | |
| NM_001304717.5:c.1320+51_1320+52insTATCAGC | NP_001291646.4:n.1320+51_1320+52insTATCAGC | |
| NM_001304718.2:c.210+51_210+52insTATCAGC | NP_001291647.1:n.210+51_210+52insTATCAGC | |
| NM_000314.8:c.801+51_801+52insTATCAGC MANE Select | NP_000305.3:n.801+51_801+52insTATCAGC |