Linked Data
MyVariant Identifiers:
chrX:g.135741361C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659202C>A , CM000685.2:g.136659202C>A | GRCh38 |
| NC_000023.10:g.135741361C>A , CM000685.1:g.135741361C>A | GRCh37 |
| NC_000023.9:g.135569027C>A | NCBI36 |
| NG_007280.1:g.16026C>A , LRG_141:g.16026C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*191C>A | ENSP00000512122.1:n.*191C>A | |
| ENST00000695725.1:c.*128C>A | ENSP00000512123.1:n.*128C>A | |
| ENST00000695726.1:n.2541C>A | ||
| ENST00000695729.1:n.3376C>A | ||
| ENST00000370629.7:c.573C>A MANE Select | ENSP00000359663.2:p.Ala191= | |
| ENST00000370628.2:c.510C>A | ENSP00000359662.2:p.Ala170= | |
| ENST00000370629.6:c.573C>A | ENSP00000359663.2:p.Ala191= | |
| NM_000074.2:c.573C>A , LRG_141t1:c.573C>A | NP_000065.1:p.Ala191= | |
| NM_000074.3:c.573C>A MANE Select | NP_000065.1:p.Ala191= |