Linked Data
dbSNP Id:
rs1206643157
gnomAD v3:
X-154370693-G-GGCCA
gnomAD v4:
X-154370693-G-GGCCA
MyVariant Identifiers:
chrX:g.154370693_154370694insGCCA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154370705_154370708dup , CM000685.2:g.154370705_154370708dup | GRCh38 |
| NC_000023.10:g.153599073_153599076dup , CM000685.1:g.153599073_153599076dup | GRCh37 |
| NC_000023.9:g.153252267_153252270dup | NCBI36 |
| NG_008677.1:g.1278_1281dup , LRG_745:g.1278_1281dup | |
| NG_011506.1:g.8942_8945dup | |
| NG_011506.2:g.8942_8945dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360319.9:c.373+176_373+179dup | ENSP00000353467.4:n.373+176_373+179dup | |
| ENST00000369850.10:c.373+176_373+179dup MANE Select | ENSP00000358866.3:n.373+176_373+179dup | |
| ENST00000369856.8:c.292+176_292+179dup | ENSP00000358872.4:n.292+176_292+179dup | |
| ENST00000422373.6:c.373+176_373+179dup | ENSP00000416926.2:n.373+176_373+179dup | |
| ENST00000610817.5:c.373+176_373+179dup | ENSP00000480593.2:n.373+176_373+179dup | |
| ENST00000676696.1:c.373+176_373+179dup | ENSP00000503392.1:n.373+176_373+179dup | |
| ENST00000344736.8:c.373+176_373+179dup | ENSP00000358863.3:n.373+176_373+179dup | |
| ENST00000360319.8:c.373+176_373+179dup | ENSP00000353467.4:n.373+176_373+179dup | |
| ENST00000369850.7:c.373+176_373+179dup | ENSP00000358866.3:n.373+176_373+179dup | |
| ENST00000369856.7:c.292+176_292+179dup | ENSP00000358872.4:n.292+176_292+179dup | |
| ENST00000420627.5:c.331+176_331+179dup | ENSP00000408921.1:n.331+176_331+179dup | |
| ENST00000422373.5:c.373+176_373+179dup | ENSP00000416926.1:n.373+176_373+179dup | |
| ENST00000610817.4:c.292+176_292+179dup | ENSP00000480593.1:n.292+176_292+179dup | |
| NM_001110556.1:c.373+176_373+179dup | NP_001104026.1:n.373+176_373+179dup | |
| NM_001456.3:c.373+176_373+179dup | NP_001447.2:n.373+176_373+179dup | |
| XM_011531127.1:c.373+176_373+179dup | XP_011529429.1:n.373+176_373+179dup | |
| XM_011531128.1:c.373+176_373+179dup | XP_011529430.1:n.373+176_373+179dup | |
| XM_011531129.1:c.373+176_373+179dup | XP_011529431.1:n.373+176_373+179dup | |
| XM_011531130.1:c.373+176_373+179dup | XP_011529432.1:n.373+176_373+179dup | |
| XM_011531131.1:c.373+176_373+179dup | XP_011529433.1:n.373+176_373+179dup | |
| NM_001110556.2:c.373+176_373+179dup MANE Select | NP_001104026.1:n.373+176_373+179dup | |
| NM_001456.4:c.373+176_373+179dup | NP_001447.2:n.373+176_373+179dup |