Linked Data
dbSNP Id:
rs1472195662
gnomAD v3:
X-149496556-T-TAGA
gnomAD v4:
X-149496556-T-TAGA
MyVariant Identifiers:
chrX:g.149496556_149496557insAGA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.149496558_149496559insAAG , CM000685.2:g.149496558_149496559insAAG | GRCh38 |
| NC_000023.10:g.148578089_148578090insAAG , CM000685.1:g.148578089_148578090insAAG | GRCh37 |
| NC_000023.9:g.148385994_148385995insAAG | NCBI36 |
| NG_011900.3:g.13778_13779insTCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340855.11:c.709-41_709-40insTCT MANE Select | ENSP00000339801.6:n.709-41_709-40insTCT | |
| ENST00000651111.1:c.76-41_76-40insTCT | ENSP00000498395.1:n.76-41_76-40insTCT | |
| ENST00000340855.10:c.709-41_709-40insTCT | ENSP00000339801.6:n.709-41_709-40insTCT | |
| ENST00000370441.8:c.709-41_709-40insTCT | ENSP00000359470.4:n.709-41_709-40insTCT | |
| ENST00000422081.6:c.76-41_76-40insTCT | ENSP00000477056.1:n.76-41_76-40insTCT | |
| ENST00000441880.1:n.114-9459_114-9458insTCT | ||
| ENST00000464251.5:c.635-41_635-40insTCT | ENSP00000428980.1:n.635-41_635-40insTCT | |
| ENST00000466019.1:n.161-41_161-40insTCT | ||
| ENST00000466323.5:c.709-41_709-40insTCT | ENSP00000418264.1:n.709-41_709-40insTCT | |
| ENST00000490775.5:n.494-41_494-40insTCT | ||
| NM_000202.6:c.709-41_709-40insTCT | NP_000193.1:n.709-41_709-40insTCT | |
| NM_001166550.2:c.439-41_439-40insTCT | NP_001160022.1:n.439-41_439-40insTCT | |
| NM_006123.4:c.709-41_709-40insTCT | NP_006114.1:n.709-41_709-40insTCT | |
| NR_104128.1:n.926-41_926-40insTCT | ||
| NM_000202.7:c.709-41_709-40insTCT | NP_000193.1:n.709-41_709-40insTCT | |
| NM_001166550.3:c.439-41_439-40insTCT | NP_001160022.1:n.439-41_439-40insTCT | |
| NM_000202.8:c.709-41_709-40insTCT MANE Select | NP_000193.1:n.709-41_709-40insTCT | |
| NM_001166550.4:c.439-41_439-40insTCT | NP_001160022.1:n.439-41_439-40insTCT | |
| NM_006123.5:c.709-41_709-40insTCT | NP_006114.1:n.709-41_709-40insTCT | |
| NR_104128.2:n.878-41_878-40insTCT |