Linked Data
ClinVar Variation Id:
1131078
ClinVar RCV Id:
RCV001464817
dbSNP Id:
rs2148127980
gnomAD v4:
X-154379530-C-T
MyVariant Identifiers:
chrX:g.153607890C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379530C>T , CM000685.2:g.154379530C>T | GRCh38 |
| NC_000023.10:g.153607890C>T , CM000685.1:g.153607890C>T | GRCh37 |
| NC_000023.9:g.153261084C>T | NCBI36 |
| NG_008677.1:g.10095C>T , LRG_745:g.10095C>T | |
| NG_011506.1:g.117G>A | |
| NG_011506.2:g.109G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682114.1:c.46C>T | ENSP00000507245.1:p.Leu16= | |
| ENST00000682478.1:n.22C>T | ||
| ENST00000683576.1:n.22C>T | ||
| ENST00000683627.1:c.46C>T | ENSP00000507533.1:p.Leu16= | |
| ENST00000684082.1:c.46C>T | ENSP00000508266.1:p.Leu16= | |
| ENST00000684633.1:n.22C>T | ||
| ENST00000684678.1:c.46C>T | ENSP00000507059.1:p.Leu16= | |
| ENST00000369842.9:c.46C>T MANE Select | ENSP00000358857.4:p.Leu16= | |
| ENST00000369835.3:c.46C>T | ENSP00000358850.3:p.Leu16= | |
| ENST00000369842.8:c.46C>T | ENSP00000358857.4:p.Leu16= | |
| ENST00000428228.5:c.46C>T | ENSP00000401081.1:p.Leu16= | |
| ENST00000468294.5:n.6C>T | ||
| ENST00000485261.1:n.127C>T | ||
| ENST00000486738.5:n.190C>T | ||
| ENST00000494443.5:n.103C>T | ||
| NM_000117.2:c.46C>T , LRG_745t1:c.46C>T | NP_000108.1:p.Leu16= | |
| XM_024452349.1:c.-163C>T | XP_024308117.1:n.-163C>T | |
| NM_000117.3:c.46C>T MANE Select | NP_000108.1:p.Leu16= |