Linked Data
dbSNP Id:
rs1569552095
gnomAD v2:
X-153609086-TCCCCTCGCCCTGACTC-T
MyVariant Identifiers:
chrX:g.153609087_153609102del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154380727_154380742del , CM000685.2:g.154380727_154380742del | GRCh38 |
| NC_000023.10:g.153609087_153609102del , CM000685.1:g.153609087_153609102del | GRCh37 |
| NC_000023.9:g.153262281_153262296del | NCBI36 |
| NG_008677.1:g.11292_11307del , LRG_745:g.11292_11307del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682114.1:c.400-26_400-11del | ENSP00000507245.1:n.400-26_400-11del | |
| ENST00000682478.1:n.590-26_590-11del | ||
| ENST00000683576.1:n.590-26_590-11del | ||
| ENST00000683627.1:c.400-26_400-11del | ENSP00000507533.1:n.400-26_400-11del | |
| ENST00000684082.1:c.357-26_357-11del | ENSP00000508266.1:n.357-26_357-11del | |
| ENST00000684633.1:n.372-26_372-11del | ||
| ENST00000684678.1:c.396-26_396-11del | ENSP00000507059.1:n.396-26_396-11del | |
| ENST00000369842.9:c.400-26_400-11del MANE Select | ENSP00000358857.4:n.400-26_400-11del | |
| ENST00000369835.3:c.295-26_295-11del | ENSP00000358850.3:n.295-26_295-11del | |
| ENST00000369842.8:c.400-26_400-11del | ENSP00000358857.4:n.400-26_400-11del | |
| ENST00000428228.5:c.*305-26_*305-11del | ENSP00000401081.1:n.*305-26_*305-11del | |
| ENST00000468294.5:n.360-26_360-11del | ||
| ENST00000471965.1:n.163_178del | ||
| ENST00000485261.1:n.590-26_590-11del | ||
| ENST00000486738.5:n.758-26_758-11del | ||
| ENST00000492448.1:n.383-26_383-11del | ||
| NM_000117.2:c.400-26_400-11del , LRG_745t1:c.400-26_400-11del | NP_000108.1:n.400-26_400-11del | |
| XM_024452349.1:c.406-26_406-11del | XP_024308117.1:n.406-26_406-11del | |
| NM_000117.3:c.400-26_400-11del MANE Select | NP_000108.1:n.400-26_400-11del |