Linked Data
dbSNP Id:
rs1567311251
gnomAD v2:
15-48521531-T-TTTAGG
MyVariant Identifiers:
chr15:g.48521532delinsTTAGGA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48229334_48229335insTTAGG , CM000677.2:g.48229334_48229335insTTAGG | GRCh38 |
| NC_000015.9:g.48521531_48521532insTTAGG , CM000677.1:g.48521531_48521532insTTAGG | GRCh37 |
| NC_000015.8:g.46308823_46308824insTTAGG | NCBI36 |
| NG_021301.1:g.28034_28035insTTAGG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000686073.1:c.864+6_864+7insTTAGG | ENSP00000508901.1:n.864+6_864+7insTTAGG | |
| ENST00000380993.8:c.864+6_864+7insTTAGG MANE Select | ENSP00000370381.3:n.864+6_864+7insTTAGG | |
| ENST00000646012.1:c.1002+6_1002+7insTTAGG | ENSP00000495813.1:n.1002+6_1002+7insTTAGG... | |
| ENST00000647232.1:c.864+6_864+7insTTAGG | ENSP00000493875.1:n.864+6_864+7insTTAGG | |
| ENST00000647546.1:c.864+6_864+7insTTAGG | ENSP00000495332.1:n.864+6_864+7insTTAGG | |
| ENST00000330289.10:c.864+6_864+7insTTAGG | ENSP00000331550.6:n.864+6_864+7insTTAGG | |
| ENST00000380993.7:c.864+6_864+7insTTAGG | ENSP00000370381.3:n.864+6_864+7insTTAGG | |
| ENST00000396577.7:c.864+6_864+7insTTAGG | ENSP00000379822.3:n.864+6_864+7insTTAGG | |
| ENST00000558252.5:n.4987+6_4987+7insTTAGG | ||
| ENST00000558405.5:c.864+6_864+7insTTAGG | ENSP00000453409.1:n.864+6_864+7insTTAGG | |
| ENST00000559641.5:c.303+6_303+7insTTAGG | ENSP00000453230.1:n.303+6_303+7insTTAGG | |
| ENST00000559723.2:n.237+6_237+7insTTAGG | ||
| ENST00000560692.5:n.5003+6_5003+7insTTAGG | ||
| ENST00000561127.5:c.303+6_303+7insTTAGG | ENSP00000453602.2:n.303+6_303+7insTTAGG | |
| NM_000338.2:c.864+6_864+7insTTAGG | NP_000329.2:n.864+6_864+7insTTAGG | |
| NM_001184832.1:c.864+6_864+7insTTAGG | NP_001171761.1:n.864+6_864+7insTTAGG | |
| XM_005254605.1:c.960+6_960+7insTTAGG | XP_005254662.1:n.960+6_960+7insTTAGG | |
| XM_005254606.1:c.864+6_864+7insTTAGG | XP_005254663.1:n.864+6_864+7insTTAGG | |
| XM_006720656.1:c.960+6_960+7insTTAGG | XP_006720719.1:n.960+6_960+7insTTAGG | |
| XR_931896.1:n.1176+6_1176+7insTTAGG | ||
| XR_932203.1:n.229+621_229+622insCCTAA | ||
| XR_932204.1:n.222+621_222+622insCCTAA | ||
| XM_005254606.2:c.864+6_864+7insTTAGG | XP_005254663.1:n.864+6_864+7insTTAGG | |
| XR_001751524.2:n.230+621_230+622insCCTAA | ||
| XR_001751525.1:n.230+621_230+622insCCTAA | ||
| XR_002957762.1:n.230+621_230+622insCCTAA | ||
| XR_932204.3:n.224+621_224+622insCCTAA | ||
| NM_000338.3:c.864+6_864+7insTTAGG MANE Select | NP_000329.2:n.864+6_864+7insTTAGG | |
| NM_001184832.2:c.864+6_864+7insTTAGG | NP_001171761.1:n.864+6_864+7insTTAGG | |
| NM_001384136.1:c.864+6_864+7insTTAGG | NP_001371065.1:n.864+6_864+7insTTAGG |