Linked Data
ClinVar Variation Id:
2851451
ClinVar RCV Id:
RCV003691152
gnomAD v4:
X-108606774-T-A
MyVariant Identifiers:
chrX:g.107850004T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108606774T>A , CM000685.2:g.108606774T>A | GRCh38 |
| NC_000023.10:g.107850004T>A , CM000685.1:g.107850004T>A | GRCh37 |
| NC_000023.9:g.107736660T>A | NCBI36 |
| NG_011977.1:g.171851T>A | |
| NG_011977.2:g.171851T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328300.11:c.2277T>A MANE Select | ENSP00000331902.7:p.Pro759= | |
| ENST00000361603.7:c.2277T>A | ENSP00000354505.2:p.Pro759= | |
| ENST00000328300.10:c.2277T>A | ENSP00000331902.6:p.Pro759= | |
| ENST00000361603.6:c.2277T>A | ENSP00000354505.2:p.Pro759= | |
| ENST00000483338.1:n.1733T>A | ||
| NM_000495.4:c.2277T>A | NP_000486.1:p.Pro759= | |
| NM_033380.2:c.2277T>A | NP_203699.1:p.Pro759= | |
| XM_005262070.2:c.2277T>A | XP_005262127.1:p.Pro759= | |
| XM_005262072.3:c.2277T>A | XP_005262129.1:p.Pro759= | |
| XM_006724616.2:c.2277T>A | XP_006724679.1:p.Pro759= | |
| XM_011530849.1:c.1953T>A | XP_011529151.1:p.Pro651= | |
| XM_011530850.1:c.2277T>A | XP_011529152.1:p.Pro759= | |
| XM_011530851.1:c.-33+3713T>A | XP_011529153.1:n.-33+3713T>A | |
| XM_011530849.2:c.2292T>A | XP_011529151.2:p.Pro764= | |
| XM_017029259.2:c.2292T>A | XP_016884748.1:p.Pro764= | |
| XM_017029260.1:c.2292T>A | XP_016884749.1:p.Pro764= | |
| XM_017029261.1:c.2292T>A | XP_016884750.1:p.Pro764= | |
| XM_017029262.2:c.2292T>A | XP_016884751.1:p.Pro764= | |
| XM_017029263.2:c.612T>A | XP_016884752.1:p.Pro204= | |
| NM_000495.5:c.2277T>A | NP_000486.1:p.Pro759= | |
| NM_033380.3:c.2277T>A MANE Select | NP_203699.1:p.Pro759= |