Linked Data
ClinVar Variation Id:
802630
ClinVar RCV Id:
RCV000988445
dbSNP Id:
rs1589969829
gnomAD v2:
10-104263945-CACCGCG-C
gnomAD v3:
10-102504188-CACCGCG-C
gnomAD v4:
10-102504188-CACCGCG-C
MyVariant Identifiers:
chr10:g.104263946_104263951del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102504189_102504194del , CM000672.2:g.102504189_102504194del | GRCh38 |
| NC_000010.10:g.104263946_104263951del , CM000672.1:g.104263946_104263951del | GRCh37 |
| NC_000010.9:g.104253936_104253941del | NCBI36 |
| NG_011901.1:g.3562_3567del | |
| NG_021338.1:g.5228_5233del , LRG_521:g.5228_5233del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369902.8:c.37_42del MANE Select | ENSP00000358918.4:p.Thr13_Ala14del | |
| ENST00000369899.6:c.37_42del | ENSP00000358915.2:p.Thr13_Ala14del | |
| ENST00000369902.7:c.37_42del | ENSP00000358918.3:p.Thr13_Ala14del | |
| ENST00000423559.2:c.37_42del | ENSP00000411597.2:p.Thr13_Ala14del | |
| NM_001178133.1:c.37_42del | NP_001171604.1:p.Thr13_Ala14del | |
| NM_016169.3:c.37_42del , LRG_521t1:c.37_42del | NP_057253.2:p.Thr13_Ala14del | |
| XM_011539858.1:c.37_42del | XP_011538160.1:p.Thr13_Ala14del | |
| XM_011539859.1:c.37_42del | XP_011538161.1:p.Thr13_Ala14del | |
| XM_011539860.1:c.37_42del | XP_011538162.1:p.Thr13_Ala14del | |
| XM_011539861.1:c.37_42del | XP_011538163.1:p.Thr13_Ala14del | |
| XM_011539863.1:c.8+1203_8+1208del | XP_011538165.1:n.8+1203_8+1208del | |
| XM_011539864.1:c.37_42del | XP_011538166.1:p.Thr13_Ala14del | |
| XM_011539858.3:c.37_42del | XP_011538160.1:p.Thr13_Ala14del | |
| XM_011539860.3:c.37_42del | XP_011538162.1:p.Thr13_Ala14del | |
| XM_011539861.3:c.37_42del | XP_011538163.1:p.Thr13_Ala14del | |
| XM_011539863.3:c.8+1203_8+1208del | XP_011538165.1:n.8+1203_8+1208del | |
| XM_011539864.3:c.37_42del | XP_011538166.1:p.Thr13_Ala14del | |
| NM_001178133.2:c.37_42del | NP_001171604.1:p.Thr13_Ala14del | |
| NM_016169.4:c.37_42del MANE Select | NP_057253.2:p.Thr13_Ala14del |