Linked Data
ClinVar Variation Id:
1144443
ClinVar RCV Id:
RCV001482973
dbSNP Id:
rs1433326581
MyVariant Identifiers:
chrX:g.138644191G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139562032G>A , CM000685.2:g.139562032G>A | GRCh38 |
| NC_000023.10:g.138644191G>A , CM000685.1:g.138644191G>A | GRCh37 |
| NC_000023.9:g.138471857G>A | NCBI36 |
| NG_007994.1:g.36297G>A , LRG_556:g.36297G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.1347G>A MANE Select | ENSP00000218099.2:p.Arg449= | |
| ENST00000643157.1:n.1723+291G>A | ||
| ENST00000218099.6:c.1347G>A | ENSP00000218099.2:p.Arg449= | |
| ENST00000394090.2:c.1233G>A | ENSP00000377650.2:p.Arg411= | |
| NM_000133.3:c.1347G>A , LRG_556t1:c.1347G>A | NP_000124.1:p.Arg449= | |
| NM_001313913.1:c.1233G>A | NP_001300842.1:p.Arg411= | |
| XM_005262397.3:c.1218G>A | XP_005262454.1:p.Arg406= | |
| XM_005262397.4:c.1218G>A | XP_005262454.1:p.Arg406= | |
| NM_000133.4:c.1347G>A MANE Select | NP_000124.1:p.Arg449= | |
| NM_001313913.2:c.1233G>A | NP_001300842.1:p.Arg411= |