Linked Data
dbSNP Id:
rs1564627643
gnomAD v2:
10-79793619-TTC-T
gnomAD v4:
10-78033861-TTC-T
MyVariant Identifiers:
chr10:g.79793620_79793621del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.78033865_78033866del , CM000672.2:g.78033865_78033866del | GRCh38 |
| NC_000010.10:g.79793623_79793624del , CM000672.1:g.79793623_79793624del | GRCh37 |
| NC_000010.9:g.79463629_79463630del | NCBI36 |
| NG_012633.1:g.5106_5107del | |
| NG_029648.1:g.678_679del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613865.5:c.-37_-36del | ENSP00000478869.2:n.-37_-36del | |
| ENST00000645440.1:c.-37_-36del | ENSP00000496738.1:n.-37_-36del | |
| ENST00000435275.5:c.-37_-36del | ENSP00000415549.1:n.-37_-36del | |
| ENST00000440692.5:c.-37_-36del | ENSP00000414321.1:n.-37_-36del | |
| ENST00000485708.6:n.22_23del | ||
| ENST00000613865.4:c.-37_-36del | ENSP00000478869.1:n.-37_-36del | |
| NM_001026.4:c.-37_-36del | NP_001017.1:n.-37_-36del | |
| NM_001142282.1:c.-37_-36del | NP_001135754.1:n.-37_-36del | |
| NM_001142283.1:c.-37_-36del | NP_001135755.1:n.-37_-36del | |
| NM_001142284.1:c.-37_-36del | NP_001135756.1:n.-37_-36del | |
| NM_001142285.1:c.-37_-36del | NP_001135757.1:n.-37_-36del | |
| NM_033022.3:c.-37_-36del | NP_148982.1:n.-37_-36del |