Linked Data
ClinVar Variation Id:
1137279
ClinVar RCV Id:
RCV001473206
dbSNP Id:
rs1557340286
gnomAD v3:
X-149503478-G-A
gnomAD v4:
X-149503478-G-A
MyVariant Identifiers:
chrX:g.148585008G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.149503478G>A , CM000685.2:g.149503478G>A | GRCh38 |
| NC_000023.10:g.148585008G>A , CM000685.1:g.148585008G>A | GRCh37 |
| NC_000023.9:g.148392913G>A | NCBI36 |
| NG_011900.3:g.6857C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340855.11:c.252C>T MANE Select | ENSP00000339801.6:p.Cys84= | |
| ENST00000651111.1:c.-215-2441C>T | ENSP00000498395.1:n.-215-2441C>T | |
| ENST00000340855.10:c.252C>T | ENSP00000339801.6:p.Cys84= | |
| ENST00000370441.8:c.252C>T | ENSP00000359470.4:p.Cys84= | |
| ENST00000422081.6:c.-215-2441C>T | ENSP00000477056.1:n.-215-2441C>T | |
| ENST00000427113.2:n.770-1255C>T | ||
| ENST00000428056.6:c.252C>T | ENSP00000390241.2:p.Cys84= | |
| ENST00000441880.1:n.114-16380C>T | ||
| ENST00000464251.5:c.75C>T | ENSP00000428980.1:p.Cys25= | |
| ENST00000466323.5:c.252C>T | ENSP00000418264.1:p.Cys84= | |
| ENST00000521702.1:c.252C>T | ENSP00000429745.1:p.Cys84= | |
| ENST00000523759.5:n.533-2441C>T | ||
| NM_000202.6:c.252C>T | NP_000193.1:p.Cys84= | |
| NM_001166550.2:c.15-33C>T | NP_001160022.1:n.15-33C>T | |
| NM_006123.4:c.252C>T | NP_006114.1:p.Cys84= | |
| NR_104128.1:n.469C>T | ||
| NM_000202.7:c.252C>T | NP_000193.1:p.Cys84= | |
| NM_001166550.3:c.15-33C>T | NP_001160022.1:n.15-33C>T | |
| NM_000202.8:c.252C>T MANE Select | NP_000193.1:p.Cys84= | |
| NM_001166550.4:c.15-33C>T | NP_001160022.1:n.15-33C>T | |
| NM_006123.5:c.252C>T | NP_006114.1:p.Cys84= | |
| NR_104128.2:n.421C>T |