Linked Data
dbSNP Id:
rs1448095177
gnomAD v3:
10-87965040-AAAAT-A
gnomAD v4:
10-87965040-AAAAT-A
MyVariant Identifiers:
chr10:g.87965041_87965044del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87965049_87965052del , CM000672.2:g.87965049_87965052del | GRCh38 |
| NC_000010.10:g.89724806_89724809del , CM000672.1:g.89724806_89724809del | GRCh37 |
| NC_000010.9:g.89714786_89714789del | NCBI36 |
| NG_007466.2:g.106611_106614del , LRG_311:g.106611_106614del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.1120-238_1120-235del | ENSP00000514759.2:n.1120-238_1120-235del | |
| ENST00000710265.1:c.*56-238_*56-235del | ENSP00000518161.1:n.*56-238_*56-235del | |
| ENST00000688158.2:n.1762-238_1762-235del | ||
| ENST00000688922.2:c.*857-238_*857-235del | ENSP00000508742.2:n.*857-238_*857-235del | |
| ENST00000700021.1:c.982-238_982-235del | ENSP00000514757.1:n.982-238_982-235del | |
| ENST00000700022.1:c.*366-238_*366-235del | ENSP00000514758.1:n.*366-238_*366-235del | |
| ENST00000700023.1:n.2185-238_2185-235del | ||
| ENST00000700024.1:n.2419-238_2419-235del | ||
| ENST00000706954.1:c.1027-238_1027-235del | ENSP00000516674.1:n.1027-238_1027-235del | |
| ENST00000706955.1:c.*1062-238_*1062-235del | ENSP00000516675.1:n.*1062-238_*1062-235del | |
| ENST00000686459.1:c.*613-238_*613-235del | ENSP00000508909.1:n.*613-238_*613-235del | |
| ENST00000688158.1:c.*1138-238_*1138-235del | ENSP00000509254.1:n.*1138-238_*1138-235del | |
| ENST00000688308.1:c.1027-238_1027-235del | ENSP00000508752.1:n.1027-238_1027-235del | |
| ENST00000688922.1:c.948-238_948-235del | ||
| ENST00000693560.1:c.1546-238_1546-235del | ENSP00000509861.1:n.1546-238_1546-235del | |
| ENST00000371953.8:c.1027-238_1027-235del MANE Select | ENSP00000361021.3:n.1027-238_1027-235del | |
| ENST00000371953.7:c.1027-238_1027-235del | ENSP00000361021.3:n.1027-238_1027-235del | |
| NM_000314.5:c.1027-238_1027-235del | NP_000305.3:n.1027-238_1027-235del | |
| NM_000314.6:c.1027-238_1027-235del | NP_000305.3:n.1027-238_1027-235del | |
| NM_001304717.2:c.1546-238_1546-235del | NP_001291646.2:n.1546-238_1546-235del | |
| NM_001304718.1:c.436-238_436-235del | NP_001291647.1:n.436-238_436-235del | |
| XM_006717926.2:c.982-238_982-235del | XP_006717989.1:n.982-238_982-235del | |
| XM_011539982.1:c.931-238_931-235del | XP_011538284.1:n.931-238_931-235del | |
| XR_945791.1:n.1597-238_1597-235del | ||
| NM_000314.7:c.1027-238_1027-235del | NP_000305.3:n.1027-238_1027-235del | |
| NM_001304717.5:c.1546-238_1546-235del | NP_001291646.4:n.1546-238_1546-235del | |
| NM_001304718.2:c.436-238_436-235del | NP_001291647.1:n.436-238_436-235del | |
| NM_000314.8:c.1027-238_1027-235del MANE Select | NP_000305.3:n.1027-238_1027-235del |