Linked Data
dbSNP Id:
rs1557229920
gnomAD v2:
X-153761332-C-T
gnomAD v4:
X-154533117-C-T
MyVariant Identifiers:
chrX:g.153761332C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154533117C>T , CM000685.2:g.154533117C>T | GRCh38 |
| NC_000023.10:g.153761332C>T , CM000685.1:g.153761332C>T | GRCh37 |
| NC_000023.9:g.153414526C>T | NCBI36 |
| NG_009015.2:g.19456G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393564.7:c.876G>A | ENSP00000377194.2:p.Leu292= | |
| ENST00000439227.6:c.879G>A | ENSP00000395599.2:p.Leu293= | |
| ENST00000696420.1:c.876G>A | ENSP00000512615.1:p.Leu292= | |
| ENST00000696421.1:c.876G>A | ENSP00000512616.1:p.Leu292= | |
| ENST00000696422.1:c.739G>A | ||
| ENST00000696423.1:c.742G>A | ||
| ENST00000696424.1:c.728G>A | ENSP00000512619.1:p.Ter243= | |
| ENST00000696425.1:c.865-315G>A | ENSP00000512620.1:n.865-315G>A | |
| ENST00000696426.1:c.*336G>A | ENSP00000512621.1:n.*336G>A | |
| ENST00000696427.1:c.883G>A | ENSP00000512622.1:p.Glu295Lys | |
| ENST00000696428.1:c.*718G>A | ENSP00000512623.1:n.*718G>A | |
| ENST00000696429.1:c.876G>A | ENSP00000512624.1:p.Leu292= | |
| ENST00000696430.1:c.876G>A | ENSP00000512625.1:p.Leu292= | |
| ENST00000393562.10:c.876G>A MANE Select | ENSP00000377192.3:p.Leu292= | |
| ENST00000369620.6:c.1014G>A | ENSP00000358633.2:p.Leu338= | |
| ENST00000393562.6:c.966G>A | ENSP00000377192.2:p.Leu322= | |
| ENST00000393564.6:c.876G>A | ENSP00000377194.2:p.Leu292= | |
| ENST00000439227.5:c.879G>A | ENSP00000395599.1:p.Leu293= | |
| ENST00000440967.5:c.879G>A | ENSP00000400648.1:p.Leu293= | |
| ENST00000621232.4:c.876G>A | ENSP00000483686.1:p.Leu292= | |
| NM_000402.4:c.966G>A | NP_000393.4:p.Leu322= | |
| NM_001042351.2:c.876G>A | NP_001035810.1:p.Leu292= | |
| XM_005274657.2:c.969G>A | XP_005274714.1:p.Leu323= | |
| XM_005274658.2:c.879G>A | XP_005274715.1:p.Leu293= | |
| XM_011531132.1:c.958-315G>A | XP_011529434.1:n.958-315G>A | |
| NM_001360016.2:c.876G>A MANE Select | NP_001346945.1:p.Leu292= | |
| NM_001042351.3:c.876G>A | NP_001035810.1:p.Leu292= |