Linked Data
dbSNP Id:
rs2063908242
gnomAD v3:
X-41345243-A-G
gnomAD v4:
X-41345243-A-G
MyVariant Identifiers:
chrX:g.41204496A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.41345243A>G , CM000685.2:g.41345243A>G | GRCh38 |
| NC_000023.10:g.41204496A>G , CM000685.1:g.41204496A>G | GRCh37 |
| NC_000023.9:g.41089440A>G | NCBI36 |
| NG_012830.1:g.16846A>G | |
| NG_012830.2:g.16846A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642322.2:c.1221A>G | ENSP00000496052.2:p.Arg407= | |
| ENST00000399959.7:c.1086A>G | ENSP00000382840.3:p.Arg362= | |
| ENST00000441189.4:c.990A>G | ENSP00000414281.3:p.Arg330= | |
| ENST00000457138.7:c.1041A>G | ENSP00000392494.2:p.Arg347= | |
| ENST00000629496.3:c.1089A>G | ENSP00000487224.1:p.Arg363= | |
| ENST00000642161.1:n.3288A>G | ||
| ENST00000642322.1:c.531A>G | ENSP00000496052.1:p.Arg177= | |
| ENST00000642424.1:c.531A>G | ENSP00000496356.1:p.Arg177= | |
| ENST00000642589.1:n.4411A>G | ||
| ENST00000642597.1:n.1263A>G | ||
| ENST00000642687.1:n.1122A>G | ||
| ENST00000642722.1:n.1922A>G | ||
| ENST00000642763.1:n.1980A>G | ||
| ENST00000642793.1:c.*538A>G | ENSP00000493976.1:n.*538A>G | |
| ENST00000642801.1:n.738A>G | ||
| ENST00000643820.1:n.365A>G | ||
| ENST00000643963.1:c.*371A>G | ENSP00000495264.1:n.*371A>G | |
| ENST00000644073.1:c.1047A>G | ENSP00000493475.1:p.Arg349= | |
| ENST00000644074.1:c.1086A>G | ENSP00000496663.1:p.Arg362= | |
| ENST00000644109.1:c.1251A>G | ENSP00000494952.1:p.Arg417= | |
| ENST00000644307.1:n.1180A>G | ||
| ENST00000644513.1:c.1089A>G | ENSP00000493819.1:p.Arg363= | |
| ENST00000644677.1:c.972A>G | ENSP00000496524.1:p.Arg324= | |
| ENST00000644876.2:c.1089A>G MANE Select | ENSP00000494040.1:p.Arg363= | |
| ENST00000644958.1:n.2750A>G | ||
| ENST00000645080.1:c.*2311A>G | ENSP00000494767.1:n.*2311A>G | |
| ENST00000645120.1:n.2584A>G | ||
| ENST00000645338.1:n.1180A>G | ||
| ENST00000645380.1:n.2474A>G | ||
| ENST00000645561.1:n.2265A>G | ||
| ENST00000645574.1:n.3953A>G | ||
| ENST00000645589.1:c.1089A>G | ENSP00000494588.1:p.Arg363= | |
| ENST00000646093.1:n.273A>G | ||
| ENST00000646107.1:c.972A>G | ENSP00000494518.1:p.Arg324= | |
| ENST00000646122.1:c.1089A>G | ENSP00000496222.1:p.Arg363= | |
| ENST00000646196.1:n.2058A>G | ||
| ENST00000646223.1:c.*1082A>G | ENSP00000496043.1:n.*1082A>G | |
| ENST00000646319.1:c.1089A>G | ENSP00000495377.1:p.Arg363= | |
| ENST00000646390.1:n.3377A>G | ||
| ENST00000646627.1:c.531A>G | ENSP00000493795.1:p.Arg177= | |
| ENST00000646679.1:c.531A>G | ENSP00000494887.1:p.Arg177= | |
| ENST00000646822.1:n.2151A>G | ||
| ENST00000646940.1:n.1263A>G | ||
| ENST00000647286.1:n.1187A>G | ||
| ENST00000399959.6:c.1089A>G | ENSP00000382840.2:p.Arg363= | |
| ENST00000441189.3:c.341-2397A>G | ENSP00000414281.2:n.341-2397A>G | |
| ENST00000457138.6:c.1041A>G | ENSP00000392494.2:p.Arg347= | |
| ENST00000478993.5:c.1089A>G | ENSP00000478443.1:p.Arg363= | |
| ENST00000542215.5:n.1137A>G | ||
| ENST00000625837.2:c.1089A>G | ENSP00000486306.1:p.Arg363= | |
| ENST00000626301.2:c.1089A>G | ENSP00000486443.1:p.Arg363= | |
| ENST00000629496.2:c.1089A>G | ENSP00000487224.1:p.Arg363= | |
| ENST00000629785.2:c.1089A>G | ENSP00000486516.1:p.Arg363= | |
| ENST00000630255.2:c.1089A>G | ENSP00000486720.1:p.Arg363= | |
| ENST00000630370.2:c.1089A>G | ENSP00000487062.1:p.Arg363= | |
| ENST00000630858.2:c.1089A>G | ENSP00000486514.1:p.Arg363= | |
| NM_001193416.2:c.1089A>G | NP_001180345.1:p.Arg363= | |
| NM_001193417.2:c.1041A>G | NP_001180346.1:p.Arg347= | |
| NM_001356.4:c.1089A>G | NP_001347.3:p.Arg363= | |
| NR_126093.1:n.2034A>G | ||
| XM_011543892.1:c.1089A>G | XP_011542194.1:p.Arg363= | |
| NM_001363819.1:c.531A>G | NP_001350748.1:p.Arg177= | |
| XM_011543892.2:c.1089A>G | XP_011542194.1:p.Arg363= | |
| XM_017029313.1:c.531A>G | XP_016884802.1:p.Arg177= | |
| NM_001193416.3:c.1089A>G | NP_001180345.1:p.Arg363= | |
| NM_001193417.3:c.1041A>G | NP_001180346.1:p.Arg347= | |
| NM_001356.5:c.1089A>G MANE Select | NP_001347.3:p.Arg363= |