Linked Data
dbSNP Id:
rs1557265151
gnomAD v2:
X-154001528-A-C
gnomAD v4:
X-154773253-A-C
MyVariant Identifiers:
chrX:g.154001528A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154773253A>C , CM000685.2:g.154773253A>C | GRCh38 |
| NC_000023.10:g.154001528A>C , CM000685.1:g.154001528A>C | GRCh37 |
| NC_000023.9:g.153654722A>C | NCBI36 |
| NG_009780.1:g.15498A>C , LRG_55:g.15498A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413910.6:c.1035+4A>C | ENSP00000400542.2:n.1035+4A>C | |
| ENST00000426673.6:c.*538+4A>C | ENSP00000407253.3:n.*538+4A>C | |
| ENST00000484317.6:n.940+4A>C | ||
| ENST00000696575.1:c.1155+4A>C | ENSP00000512730.1:n.1155+4A>C | |
| ENST00000696577.1:c.1155+4A>C | ENSP00000512731.1:n.1155+4A>C | |
| ENST00000696578.1:c.*107+4A>C | ENSP00000512732.1:n.*107+4A>C | |
| ENST00000696579.1:n.1257+4A>C | ||
| ENST00000696580.1:c.1068+4A>C | ENSP00000512733.1:n.1068+4A>C | |
| ENST00000696581.1:c.*1129+4A>C | ENSP00000512734.1:n.*1129+4A>C | |
| ENST00000696582.1:c.*361+4A>C | ENSP00000512735.1:n.*361+4A>C | |
| ENST00000696583.1:c.1116+4A>C | ENSP00000512736.1:n.1116+4A>C | |
| ENST00000696584.1:n.1679+4A>C | ||
| ENST00000696585.1:n.1798+4A>C | ||
| ENST00000696586.1:n.1572+4A>C | ||
| ENST00000696587.1:c.1035+4A>C | ENSP00000512737.1:n.1035+4A>C | |
| ENST00000696588.1:c.546+4A>C | ENSP00000513251.1:n.546+4A>C | |
| ENST00000696589.1:n.930+4A>C | ||
| ENST00000696590.1:n.779+4A>C | ||
| ENST00000696591.1:n.504+4A>C | ||
| ENST00000696592.1:n.2034+4A>C | ||
| ENST00000696627.1:c.1159A>C | ENSP00000512764.1:p.Ile387Leu | |
| ENST00000696628.1:c.1155+4A>C | ENSP00000512765.1:n.1155+4A>C | |
| ENST00000369550.10:c.1155+4A>C MANE Select | ENSP00000358563.5:n.1155+4A>C | |
| ENST00000369550.9:c.1155+4A>C | ENSP00000358563.5:n.1155+4A>C | |
| ENST00000412124.5:c.413+4A>C | ||
| ENST00000426673.5:c.515+4A>C | ||
| ENST00000475966.1:n.644+4A>C | ||
| ENST00000481062.1:n.106+4A>C | ||
| ENST00000620277.4:c.1155+4A>C | ENSP00000478387.1:n.1155+4A>C | |
| NM_001142463.2:c.1155+4A>C | NP_001135935.1:n.1155+4A>C | |
| NM_001288747.1:c.1155+4A>C | NP_001275676.1:n.1155+4A>C | |
| NM_001363.4:c.1155+4A>C | NP_001354.1:n.1155+4A>C | |
| NR_110021.1:n.1856+4A>C | ||
| NR_110022.1:n.1975+4A>C | ||
| NR_110023.1:n.1749+4A>C | ||
| NM_001363.5:c.1155+4A>C MANE Select | NP_001354.1:n.1155+4A>C | |
| NM_001142463.3:c.1155+4A>C | NP_001135935.1:n.1155+4A>C | |
| NR_110021.2:n.1734+4A>C | ||
| NR_110022.2:n.1853+4A>C | ||
| NR_110023.2:n.1627+4A>C | ||
| NM_001288747.2:c.1155+4A>C | NP_001275676.1:n.1155+4A>C |