Linked Data
gnomAD v2:
X-154133314-G-GAAA
MyVariant Identifiers:
chrX:g.154133314_154133315insAAA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154905040_154905041insAAA , CM000685.2:g.154905040_154905041insAAA | GRCh38 |
| NC_000023.10:g.154133315_154133316insAAA , CM000685.1:g.154133315_154133316insAAA | GRCh37 |
| NC_000023.9:g.153786509_153786510insAAA | NCBI36 |
| NG_011403.1:g.122684_122685insTTT | |
| NG_011403.2:g.122684_122685insTTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5374-17_5374-16insTTT MANE Select | ENSP00000353393.4:n.5374-17_5374-16insTTT | |
| ENST00000360256.8:c.5374-17_5374-16insTTT | ENSP00000353393.4:n.5374-17_5374-16insTTT | |
| NM_000132.3:c.5374-17_5374-16insTTT | NP_000123.1:n.5374-17_5374-16insTTT | |
| XM_011531126.1:c.5269-17_5269-16insTTT | XP_011529428.1:n.5269-17_5269-16insTTT | |
| NM_000132.4:c.5374-17_5374-16insTTT MANE Select | NP_000123.1:n.5374-17_5374-16insTTT |