Linked Data
ClinVar Variation Id:
1108023
ClinVar RCV Id:
RCV001433366
dbSNP Id:
rs2147197470
MyVariant Identifiers:
chrX:g.68836273C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.69616429C>T , CM000685.2:g.69616429C>T | GRCh38 |
| NC_000023.10:g.68836273C>T , CM000685.1:g.68836273C>T | GRCh37 |
| NC_000023.9:g.68752998C>T | NCBI36 |
| NG_009809.1:g.5363C>T | |
| NG_009809.2:g.5363C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374552.9:c.121C>T MANE Select | ENSP00000363680.4:p.Leu41= | |
| ENST00000338901.4:c.121C>T | ENSP00000340611.4:p.Leu41= | |
| ENST00000374548.5:n.363C>T | ||
| ENST00000374552.8:c.121C>T | ENSP00000363680.4:p.Leu41= | |
| ENST00000374553.6:c.121C>T | ENSP00000363681.2:p.Leu41= | |
| ENST00000502251.5:n.363C>T | ||
| ENST00000524573.5:c.121C>T | ENSP00000432585.1:p.Leu41= | |
| ENST00000525810.5:c.121C>T | ENSP00000434195.1:p.Leu41= | |
| ENST00000527388.5:c.121C>T | ENSP00000434861.1:p.Leu41= | |
| ENST00000533317.5:n.363C>T | ||
| NM_001005609.1:c.121C>T | NP_001005609.1:p.Leu41= | |
| NM_001005610.3:c.121C>T | NP_001005610.2:p.Leu41= | |
| NM_001005612.2:c.121C>T | NP_001005612.2:p.Leu41= | |
| NM_001005613.3:c.121C>T | NP_001005613.1:p.Leu41= | |
| NM_001399.4:c.121C>T | NP_001390.1:p.Leu41= | |
| XM_006724630.2:c.121C>T | XP_006724693.1:p.Leu41= | |
| XM_011530885.1:c.121C>T | XP_011529187.1:p.Leu41= | |
| XM_011530885.2:c.121C>T | XP_011529187.1:p.Leu41= | |
| XM_017029336.1:c.121C>T | XP_016884825.1:p.Leu41= | |
| XM_017029337.1:c.121C>T | XP_016884826.1:p.Leu41= | |
| XR_001755660.1:n.344C>T | ||
| NM_001399.5:c.121C>T MANE Select | NP_001390.1:p.Leu41= | |
| NM_001005609.2:c.121C>T | NP_001005609.1:p.Leu41= | |
| NM_001005610.4:c.121C>T | NP_001005610.2:p.Leu41= | |
| NM_001005612.3:c.121C>T | NP_001005612.2:p.Leu41= | |
| NM_001005613.4:c.121C>T | NP_001005613.1:p.Leu41= |