Linked Data
ClinVar Variation Id:
2015125
ClinVar RCV Id:
RCV002846193
gnomAD v4:
X-154367864-G-A
MyVariant Identifiers:
chrX:g.153596232G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154367864G>A , CM000685.2:g.154367864G>A | GRCh38 |
| NC_000023.10:g.153596232G>A , CM000685.1:g.153596232G>A | GRCh37 |
| NC_000023.9:g.153249426G>A | NCBI36 |
| NG_011506.1:g.11775C>T | |
| NG_011506.2:g.11775C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360319.9:c.600C>T | ENSP00000353467.4:p.Ala200= | |
| ENST00000369850.10:c.600C>T MANE Select | ENSP00000358866.3:p.Ala200= | |
| ENST00000369856.8:c.519C>T | ENSP00000358872.4:p.Ala173= | |
| ENST00000422373.6:c.600C>T | ENSP00000416926.2:p.Ala200= | |
| ENST00000610817.5:c.600C>T | ENSP00000480593.2:p.Ala200= | |
| ENST00000676696.1:c.600C>T | ENSP00000503392.1:p.Ala200= | |
| ENST00000344736.8:c.600C>T | ENSP00000358863.3:p.Ala200= | |
| ENST00000360319.8:c.600C>T | ENSP00000353467.4:p.Ala200= | |
| ENST00000369850.7:c.600C>T | ENSP00000358866.3:p.Ala200= | |
| ENST00000369856.7:c.519C>T | ENSP00000358872.4:p.Ala173= | |
| ENST00000420627.5:c.558C>T | ENSP00000408921.1:p.Ala186= | |
| ENST00000422373.5:c.600C>T | ENSP00000416926.1:p.Ala200= | |
| ENST00000610817.4:c.519C>T | ENSP00000480593.1:p.Ala173= | |
| NM_001110556.1:c.600C>T | NP_001104026.1:p.Ala200= | |
| NM_001456.3:c.600C>T | NP_001447.2:p.Ala200= | |
| XM_011531127.1:c.600C>T | XP_011529429.1:p.Ala200= | |
| XM_011531128.1:c.600C>T | XP_011529430.1:p.Ala200= | |
| XM_011531129.1:c.600C>T | XP_011529431.1:p.Ala200= | |
| XM_011531130.1:c.600C>T | XP_011529432.1:p.Ala200= | |
| XM_011531131.1:c.600C>T | XP_011529433.1:p.Ala200= | |
| NM_001110556.2:c.600C>T MANE Select | NP_001104026.1:p.Ala200= | |
| NM_001456.4:c.600C>T | NP_001447.2:p.Ala200= |