Linked Data
dbSNP Id:
rs1603005107
gnomAD v4:
X-101356855-G-A
COSMIC:
COSM2734300
MyVariant Identifiers:
chrX:g.100611843G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101356855G>A , CM000685.2:g.101356855G>A | GRCh38 |
| NC_000023.10:g.100611843G>A , CM000685.1:g.100611843G>A | GRCh37 |
| NC_000023.9:g.100498499G>A | NCBI36 |
| NG_009616.1:g.34370C>T , LRG_128:g.34370C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000478995.2:n.1438C>T | ||
| ENST00000488970.2:n.1436C>T | ||
| ENST00000695614.1:c.1278C>T | ENSP00000512053.1:p.Asp426= | |
| ENST00000695615.1:c.1278C>T | ENSP00000512054.1:p.Asp426= | |
| ENST00000695616.1:c.*1123C>T | ENSP00000512055.1:n.*1123C>T | |
| ENST00000695617.1:c.1275C>T | ENSP00000512056.1:p.Asp425= | |
| ENST00000695618.1:c.*1027C>T | ENSP00000512058.1:n.*1027C>T | |
| ENST00000695619.1:c.*988C>T | ENSP00000512059.1:n.*988C>T | |
| ENST00000695620.1:c.*1123C>T | ENSP00000512060.1:n.*1123C>T | |
| ENST00000695621.1:c.1278C>T | ENSP00000512061.1:p.Asp426= | |
| ENST00000695622.1:c.1215C>T | ENSP00000512062.1:p.Asp405= | |
| ENST00000695623.1:c.1272C>T | ENSP00000512063.1:p.Asp424= | |
| ENST00000695624.1:n.583C>T | ||
| ENST00000695625.1:c.1278C>T | ENSP00000512064.1:p.Asp426= | |
| ENST00000695626.1:c.250C>T | ENSP00000512065.1:p.Arg84Cys | |
| ENST00000695627.1:c.291C>T | ENSP00000512066.1:p.Asp97= | |
| ENST00000695628.1:c.190+654C>T | ENSP00000512067.1:n.190+654C>T | |
| ENST00000695629.1:c.190+654C>T | ENSP00000512068.1:n.190+654C>T | |
| ENST00000695630.1:c.287C>T | ||
| ENST00000695631.1:c.114+1455C>T | ||
| ENST00000695632.1:n.295C>T | ||
| ENST00000703407.1:c.1038+1519C>T | ENSP00000512057.1:n.1038+1519C>T | |
| ENST00000308731.8:c.1278C>T MANE Select | ENSP00000308176.8:p.Asp426= | |
| ENST00000308731.7:c.1278C>T | ENSP00000308176.7:p.Asp426= | |
| ENST00000372880.5:c.1038+1519C>T | ENSP00000361971.1:n.1038+1519C>T | |
| ENST00000470329.1:n.228C>T | ||
| ENST00000618050.4:c.1278C>T | ENSP00000479125.1:p.Asp426= | |
| ENST00000621635.4:c.1380C>T | ENSP00000483570.1:p.Asp460= | |
| NM_000061.2:c.1278C>T , LRG_128t1:c.1278C>T | NP_000052.1:p.Asp426= | |
| NM_001287344.1:c.1380C>T | NP_001274273.1:p.Asp460= | |
| NM_001287345.1:c.1038+1519C>T | NP_001274274.1:n.1038+1519C>T | |
| NM_000061.3:c.1278C>T MANE Select | NP_000052.1:p.Asp426= | |
| NM_001287344.2:c.1380C>T | NP_001274273.1:p.Asp460= | |
| NM_001287345.2:c.1038+1519C>T | NP_001274274.1:n.1038+1519C>T |