Linked Data
dbSNP Id:
rs1569240345
gnomAD v2:
X-41205903-ATTG-A
gnomAD v4:
X-41346650-ATTG-A
MyVariant Identifiers:
chrX:g.41205904_41205906del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.41346653_41346655del , CM000685.2:g.41346653_41346655del | GRCh38 |
| NC_000023.10:g.41205906_41205908del , CM000685.1:g.41205906_41205908del | GRCh37 |
| NC_000023.9:g.41090850_41090852del | NCBI36 |
| NG_012830.1:g.18256_18258del | |
| NG_012830.2:g.18256_18258del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642322.2:c.1747+31_1747+33del | ENSP00000496052.2:n.1747+31_1747+33del | |
| ENST00000399959.7:c.1612+31_1612+33del | ENSP00000382840.3:n.1612+31_1612+33del | |
| ENST00000441189.4:c.1516+31_1516+33del | ENSP00000414281.3:n.1516+31_1516+33del | |
| ENST00000457138.7:c.1567+31_1567+33del | ENSP00000392494.2:n.1567+31_1567+33del | |
| ENST00000611968.2:c.209+31_209+33del | ||
| ENST00000616050.3:c.363+31_363+33del | ||
| ENST00000629496.3:c.1615+31_1615+33del | ENSP00000487224.1:n.1615+31_1615+33del | |
| ENST00000642161.1:n.3814+31_3814+33del | ||
| ENST00000642322.1:c.1057+31_1057+33del | ENSP00000496052.1:n.1057+31_1057+33del | |
| ENST00000642424.1:c.1057+31_1057+33del | ENSP00000496356.1:n.1057+31_1057+33del | |
| ENST00000642589.1:n.4937+31_4937+33del | ||
| ENST00000642597.1:n.1789+31_1789+33del | ||
| ENST00000642687.1:n.1648+31_1648+33del | ||
| ENST00000642722.1:n.2448+31_2448+33del | ||
| ENST00000642763.1:n.2506+31_2506+33del | ||
| ENST00000642793.1:c.*1064+31_*1064+33del | ENSP00000493976.1:n.*1064+31_*1064+33del | |
| ENST00000642801.1:n.1264+31_1264+33del | ||
| ENST00000643820.1:n.985+31_985+33del | ||
| ENST00000643963.1:c.*897+31_*897+33del | ENSP00000495264.1:n.*897+31_*897+33del | |
| ENST00000644073.1:c.1573+31_1573+33del | ENSP00000493475.1:n.1573+31_1573+33del | |
| ENST00000644074.1:c.1612+31_1612+33del | ENSP00000496663.1:n.1612+31_1612+33del | |
| ENST00000644109.1:c.1777+31_1777+33del | ENSP00000494952.1:n.1777+31_1777+33del | |
| ENST00000644307.1:n.1785+31_1785+33del | ||
| ENST00000644513.1:c.1615+31_1615+33del | ENSP00000493819.1:n.1615+31_1615+33del | |
| ENST00000644677.1:c.1498+31_1498+33del | ENSP00000496524.1:n.1498+31_1498+33del | |
| ENST00000644876.2:c.1615+31_1615+33del MANE Select | ENSP00000494040.1:n.1615+31_1615+33del | |
| ENST00000644958.1:n.3276+31_3276+33del | ||
| ENST00000645080.1:c.*2837+31_*2837+33del | ENSP00000494767.1:n.*2837+31_*2837+33del | |
| ENST00000645120.1:n.3110+31_3110+33del | ||
| ENST00000645338.1:n.1785+31_1785+33del | ||
| ENST00000645380.1:n.3079+31_3079+33del | ||
| ENST00000645561.1:n.2791+31_2791+33del | ||
| ENST00000645574.1:n.4479+31_4479+33del | ||
| ENST00000645589.1:c.*114+31_*114+33del | ENSP00000494588.1:n.*114+31_*114+33del | |
| ENST00000646107.1:c.1498+31_1498+33del | ENSP00000494518.1:n.1498+31_1498+33del | |
| ENST00000646122.1:c.1615+31_1615+33del | ENSP00000496222.1:n.1615+31_1615+33del | |
| ENST00000646196.1:n.2584+31_2584+33del | ||
| ENST00000646223.1:c.*1608+31_*1608+33del | ENSP00000496043.1:n.*1608+31_*1608+33del | |
| ENST00000646319.1:c.1615+31_1615+33del | ENSP00000495377.1:n.1615+31_1615+33del | |
| ENST00000646390.1:n.3903+31_3903+33del | ||
| ENST00000646627.1:c.1057+31_1057+33del | ENSP00000493795.1:n.1057+31_1057+33del | |
| ENST00000646679.1:c.1057+31_1057+33del | ENSP00000494887.1:n.1057+31_1057+33del | |
| ENST00000646822.1:n.2677+31_2677+33del | ||
| ENST00000646940.1:n.1789+31_1789+33del | ||
| ENST00000647286.1:n.1713+31_1713+33del | ||
| ENST00000647477.1:n.354+31_354+33del | ||
| ENST00000399959.6:c.1615+31_1615+33del | ENSP00000382840.2:n.1615+31_1615+33del | |
| ENST00000441189.3:c.341-987_341-985del | ENSP00000414281.2:n.341-987_341-985del | |
| ENST00000457138.6:c.1567+31_1567+33del | ENSP00000392494.2:n.1567+31_1567+33del | |
| ENST00000478993.5:c.1615+31_1615+33del | ENSP00000478443.1:n.1615+31_1615+33del | |
| ENST00000611968.1:c.57+31_57+33del | ||
| ENST00000616050.2:c.168+31_168+33del | ||
| ENST00000625837.2:c.1615+31_1615+33del | ENSP00000486306.1:n.1615+31_1615+33del | |
| ENST00000626301.2:c.1615+31_1615+33del | ENSP00000486443.1:n.1615+31_1615+33del | |
| ENST00000629496.2:c.1615+31_1615+33del | ENSP00000487224.1:n.1615+31_1615+33del | |
| ENST00000629785.2:c.1615+31_1615+33del | ENSP00000486516.1:n.1615+31_1615+33del | |
| ENST00000630255.2:c.1615+31_1615+33del | ENSP00000486720.1:n.1615+31_1615+33del | |
| ENST00000630370.2:c.1615+31_1615+33del | ENSP00000487062.1:n.1615+31_1615+33del | |
| ENST00000630858.2:c.1615+31_1615+33del | ENSP00000486514.1:n.1615+31_1615+33del | |
| NM_001193416.2:c.1615+31_1615+33del | NP_001180345.1:n.1615+31_1615+33del | |
| NM_001193417.2:c.1567+31_1567+33del | NP_001180346.1:n.1567+31_1567+33del | |
| NM_001356.4:c.1615+31_1615+33del | NP_001347.3:n.1615+31_1615+33del | |
| NR_126093.1:n.2560+31_2560+33del | ||
| XM_011543892.1:c.1615+31_1615+33del | XP_011542194.1:n.1615+31_1615+33del | |
| NM_001363819.1:c.1057+31_1057+33del | NP_001350748.1:n.1057+31_1057+33del | |
| XM_011543892.2:c.1615+31_1615+33del | XP_011542194.1:n.1615+31_1615+33del | |
| XM_017029313.1:c.1057+31_1057+33del | XP_016884802.1:n.1057+31_1057+33del | |
| NM_001193416.3:c.1615+31_1615+33del | NP_001180345.1:n.1615+31_1615+33del | |
| NM_001193417.3:c.1567+31_1567+33del | NP_001180346.1:n.1567+31_1567+33del | |
| NM_001356.5:c.1615+31_1615+33del MANE Select | NP_001347.3:n.1615+31_1615+33del |