MyVariant.info:
GRCh37
chrX:g.31496451A>T
Revel Score:
ENST00000465285
0.048
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31478334A>T , CM000685.2:g.31478334A>T | GRCh38 |
| NC_000023.10:g.31496451A>T , CM000685.1:g.31496451A>T | GRCh37 |
| NC_000023.9:g.31406372A>T | NCBI36 |
| NG_012232.1:g.1866276T>A , LRG_199:g.1866276T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.3555T>A | ENSP00000350765.3:p.Leu1185= | |
| ENST00000682238.1:c.1329T>A | ENSP00000508124.1:p.Leu443= | |
| ENST00000683450.1:n.2174T>A | ||
| ENST00000683957.1:n.2201T>A | ||
| ENST00000684130.1:c.1329T>A | ENSP00000508037.1:p.Leu443= | |
| ENST00000343523.7:c.564T>A | ENSP00000340057.4:p.Leu188= | |
| ENST00000357033.9:c.8709T>A MANE Select | ENSP00000354923.3:p.Leu2903= | |
| ENST00000619831.5:c.4677T>A | ENSP00000479270.2:p.Leu1559= | |
| ENST00000620040.5:c.1329T>A | ENSP00000478150.2:p.Leu443= | |
| ENST00000680961.1:c.1329T>A | ENSP00000506386.1:p.Leu443= | |
| ENST00000681646.1:n.2370T>A | ||
| ENST00000343523.6:c.522T>A | ENSP00000340057.3:p.Leu174= | |
| ENST00000357033.8:c.8709T>A | ENSP00000354923.3:p.Leu2903= | |
| ENST00000358062.6:c.1797T>A | ENSP00000350765.2:p.Leu599= | |
| ENST00000359836.5:c.1329T>A | ENSP00000352894.1:p.Leu443= | |
| ENST00000378677.6:c.8697T>A | ENSP00000367948.2:p.Leu2899= | |
| ENST00000378707.7:c.1329T>A | ENSP00000367979.3:p.Leu443= | |
| ENST00000445312.1:n.766T>A | ||
| ENST00000474231.5:c.1329T>A | ENSP00000417123.1:p.Leu443= | |
| ENST00000541735.5:c.1329T>A | ENSP00000444119.1:p.Leu443= | |
| ENST00000619831.4:c.8694T>A | ENSP00000479270.1:p.Leu2898= | |
| ENST00000620040.4:c.8706T>A | ENSP00000478150.1:p.Leu2902= | |
| NM_000109.3:c.8685T>A | NP_000100.2:p.Leu2895= | |
| NM_004006.2:c.8709T>A , LRG_199t1:c.8709T>A | NP_003997.1:p.Leu2903= | |
| NM_004009.3:c.8697T>A | NP_004000.1:p.Leu2899= | |
| NM_004010.3:c.8340T>A | NP_004001.1:p.Leu2780= | |
| NM_004011.3:c.4686T>A | NP_004002.2:p.Leu1562= | |
| NM_004012.3:c.4677T>A | NP_004003.1:p.Leu1559= | |
| NM_004013.2:c.1329T>A | NP_004004.1:p.Leu443= | |
| NM_004014.2:c.522T>A | NP_004005.1:p.Leu174= | |
| NM_004020.3:c.1329T>A | NP_004011.2:p.Leu443= | |
| NM_004021.2:c.1329T>A | NP_004012.1:p.Leu443= | |
| NM_004022.2:c.1329T>A | NP_004013.1:p.Leu443= | |
| NM_004023.2:c.1329T>A | NP_004014.1:p.Leu443= | |
| XM_006724468.2:c.8709T>A | XP_006724531.1:p.Leu2903= | |
| XM_006724469.2:c.8685T>A | XP_006724532.1:p.Leu2895= | |
| XM_006724470.2:c.8709T>A | XP_006724533.1:p.Leu2903= | |
| XM_006724471.2:c.8709T>A | XP_006724534.1:p.Leu2903= | |
| XM_006724472.2:c.8580T>A | XP_006724535.1:p.Leu2860= | |
| XM_006724473.2:c.8571T>A | XP_006724536.1:p.Leu2857= | |
| XM_006724474.2:c.8709T>A | XP_006724537.1:p.Leu2903= | |
| XM_006724475.2:c.8709T>A | XP_006724538.1:p.Leu2903= | |
| XM_011545467.1:c.8586T>A | XP_011543769.1:p.Leu2862= | |
| XM_011545468.1:c.8709T>A | XP_011543770.1:p.Leu2903= | |
| XM_006724469.3:c.8685T>A | XP_006724532.1:p.Leu2895= | |
| XM_006724470.3:c.8709T>A | XP_006724533.1:p.Leu2903= | |
| XM_006724474.3:c.8709T>A | XP_006724537.1:p.Leu2903= | |
| XM_011545468.2:c.8709T>A | XP_011543770.1:p.Leu2903= | |
| XM_017029328.1:c.8709T>A | XP_016884817.1:p.Leu2903= | |
| XM_017029331.1:c.2883T>A | XP_016884820.1:p.Leu961= | |
| NM_000109.4:c.8685T>A | NP_000100.3:p.Leu2895= | |
| NM_004006.3:c.8709T>A MANE Select | NP_003997.2:p.Leu2903= | |
| NM_004011.4:c.4686T>A | NP_004002.3:p.Leu1562= | |
| NM_004012.4:c.4677T>A | NP_004003.2:p.Leu1559= | |
| NM_004021.3:c.1329T>A | NP_004012.2:p.Leu443= | |
| NM_004023.3:c.1329T>A | NP_004014.2:p.Leu443= | |
| NM_004013.3:c.1329T>A | NP_004004.2:p.Leu443= | |
| NM_004014.3:c.522T>A | NP_004005.2:p.Leu174= | |
| NM_004020.4:c.1329T>A | NP_004011.3:p.Leu443= | |
| NM_004022.3:c.1329T>A | NP_004013.2:p.Leu443= |