Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18656672G>A , CM000685.2:g.18656672G>A | GRCh38 |
| NC_000023.10:g.18674792G>A , CM000685.1:g.18674792G>A | GRCh37 |
| NC_000023.9:g.18584713G>A | NCBI36 |
| NG_008659.3:g.25777C>T , LRG_702:g.25777C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000330.4:c.165C>T (RS1) MANE Select | NP_000321.1:p.Thr55= |
| ENST00000379984.4:c.165C>T (RS1) MANE Select | ENSP00000369320.3:p.Thr55= |
| NM_000330.3:c.165C>T , LRG_702t1:c.165C>T (RS1) | NP_000321.1:p.Thr55= |
| ENST00000379984.3:c.165C>T (RS1) | ENSP00000369320.3:p.Thr55= |
| XR_950484.1:n.3560+3036G>A (CDKL5) |