Linked Data
gnomAD v2:
X-70775030-T-TGTGTG
gnomAD v3:
X-71555180-T-TGTGTG
gnomAD v4:
X-71555180-T-TGTGTG
MyVariant Identifiers:
chrX:g.70775030_70775031insGTGTG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.71555180_71555181insGTGTG , CM000685.2:g.71555180_71555181insGTGTG | GRCh38 |
| NC_000023.10:g.70775030_70775031insGTGTG , CM000685.1:g.70775030_70775031insGTGTG | GRCh37 |
| NC_000023.9:g.70691755_70691756insGTGTG | NCBI36 |
| NG_015875.1:g.27119_27120insGTGTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699749.1:c.660-10_660-9insGTGTG | ENSP00000514559.1:n.660-10_660-9insGTGTG | |
| ENST00000699750.1:c.*588-10_*588-9insGTGTG | ENSP00000514560.1:n.*588-10_*588-9insGTGTG | |
| ENST00000699751.1:n.1278+588_1278+589insGTGTG | ||
| ENST00000699779.1:c.*3597-10_*3597-9insGTGTG | ENSP00000514585.1:n.*3597-10_*3597-9insGTGTG | |
| ENST00000699780.1:c.728+588_728+589insGTGTG | ENSP00000514586.1:n.728+588_728+589insGTGTG | |
| ENST00000699781.1:c.*332+588_*332+589insGTGTG | ENSP00000514587.1:n.*332+588_*332+589insGTGTG | |
| ENST00000699782.1:c.630-10_630-9insGTGTG | ENSP00000514588.1:n.630-10_630-9insGTGTG | |
| ENST00000699783.1:c.699-10_699-9insGTGTG | ENSP00000514589.1:n.699-10_699-9insGTGTG | |
| ENST00000699784.1:c.699-10_699-9insGTGTG | ENSP00000514590.1:n.699-10_699-9insGTGTG | |
| ENST00000699785.1:c.*734-10_*734-9insGTGTG | ENSP00000514591.1:n.*734-10_*734-9insGTGTG | |
| ENST00000373719.8:c.729-10_729-9insGTGTG MANE Select | ENSP00000362824.3:n.729-10_729-9insGTGTG | |
| ENST00000373701.7:c.699-10_699-9insGTGTG | ENSP00000362805.3:n.699-10_699-9insGTGTG | |
| ENST00000373719.7:c.729-10_729-9insGTGTG | ENSP00000362824.3:n.729-10_729-9insGTGTG | |
| ENST00000455587.3:n.608-10_608-9insGTGTG | ||
| ENST00000459760.1:n.106-10_106-9insGTGTG | ||
| ENST00000488174.5:n.4165+588_4165+589insGTGTG | ||
| NM_181672.2:c.729-10_729-9insGTGTG | NP_858058.1:n.729-10_729-9insGTGTG | |
| NM_181673.2:c.699-10_699-9insGTGTG | NP_858059.1:n.699-10_699-9insGTGTG | |
| XM_005262308.1:c.-220+588_-220+589insGTGTG | XP_005262365.1:n.-220+588_-220+589insGTGTG | |
| XM_017029908.1:c.-220+588_-220+589insGTGTG | XP_016885397.1:n.-220+588_-220+589insGTGTG | |
| XM_024452467.1:c.-220+588_-220+589insGTGTG | XP_024308235.1:n.-220+588_-220+589insGTGTG | |
| NM_181672.3:c.729-10_729-9insGTGTG MANE Select | NP_858058.1:n.729-10_729-9insGTGTG | |
| NM_181673.3:c.699-10_699-9insGTGTG | NP_858059.1:n.699-10_699-9insGTGTG |