Linked Data
dbSNP Id:
rs1557501
gnomAD v2:
X-153197130-C-T
gnomAD v3:
X-153931677-C-T
gnomAD v4:
X-153931677-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153931677C>T , CM000685.2:g.153931677C>T | GRCh38 |
| NC_000023.10:g.153197130C>T , CM000685.1:g.153197130C>T | GRCh37 |
| NC_000023.9:g.152850324C>T | NCBI36 |
| NG_031987.1:g.8478G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000477750.6:n.1156G>A (NAA10) | ||
| ENST00000700299.1:n.809G>A (NAA10) | ||
| ENST00000464845.6:c.386+394G>A (NAA10) MANE Select | ENSP00000417763.1:n.386+394G>A | |
| ENST00000370009.5:c.341+639G>A (NAA10) | ENSP00000359026.1:n.341+639G>A | |
| ENST00000370011.7:c.323+639G>A (NAA10) | ENSP00000359028.3:n.323+639G>A | |
| ENST00000370015.8:c.386+394G>A (NAA10) | ENSP00000359032.4:n.386+394G>A | |
| ENST00000393712.7:c.386+394G>A (NAA10) | ENSP00000377315.3:n.386+394G>A | |
| ENST00000432089.1:c.368+394G>A (NAA10) | ENSP00000413668.1:n.368+394G>A | |
| ENST00000460996.5:n.675+394G>A (NAA10) | ||
| ENST00000464845.5:c.386+394G>A (NAA10) | ENSP00000417763.1:n.386+394G>A | |
| ENST00000466877.5:n.697+394G>A (NAA10) | ||
| ENST00000467451.1:n.188+394G>A (NAA10) | ||
| ENST00000484950.5:n.605+394G>A (NAA10) | ||
| ENST00000494813.5:n.481+394G>A (ARHGAP4) | ||
| NM_001256119.1:c.341+639G>A (NAA10) | NP_001243048.1:n.341+639G>A | |
| NM_001256120.1:c.368+394G>A (NAA10) | NP_001243049.1:n.368+394G>A | |
| NM_003491.3:c.386+394G>A (NAA10) | NP_003482.1:n.386+394G>A | |
| NM_003491.4:c.386+394G>A (NAA10) MANE Select | NP_003482.1:n.386+394G>A | |
| NM_001256119.2:c.341+639G>A (NAA10) | NP_001243048.1:n.341+639G>A | |
| NM_001256120.2:c.368+394G>A (NAA10) | NP_001243049.1:n.368+394G>A |