Linked Data
MyVariant Identifiers:
chrX:g.37663225G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37803972G>A , CM000685.2:g.37803972G>A | GRCh38 |
| NC_000023.10:g.37663225G>A , CM000685.1:g.37663225G>A | GRCh37 |
| NC_000023.9:g.37548169G>A | NCBI36 |
| NG_009065.1:g.28956G>A , LRG_53:g.28956G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696170.1:c.*502G>A | ENSP00000512461.1:n.*502G>A | |
| ENST00000696171.1:c.897G>A | ENSP00000512462.1:p.Lys299= | |
| ENST00000378588.5:c.993G>A MANE Select | ENSP00000367851.4:p.Lys331= | |
| ENST00000378588.4:c.993G>A | ENSP00000367851.4:p.Lys331= | |
| ENST00000465127.1:c.171+377972G>A | ENSP00000417050.1:n.171+377972G>A | |
| ENST00000492288.1:n.418G>A | ||
| NM_000397.3:c.993G>A , LRG_53t1:c.993G>A | NP_000388.2:p.Lys331= | |
| XM_011543890.1:c.687G>A | XP_011542192.1:p.Lys229= | |
| NM_000397.4:c.993G>A MANE Select | NP_000388.2:p.Lys331= |