Revel Score:
ENST00000553055
0.142
ENST00000340802
0.234
ENST00000359794 (MANE Select)
0.234
ENST00000395233
0.234
ENST00000551804
0.234
ENST00000547587
0.234
ENST00000312352
0.234
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48145043A>T , CM000674.2:g.48145043A>T | GRCh38 |
| NC_000012.11:g.48538826A>T , CM000674.1:g.48538826A>T | GRCh37 |
| NC_000012.10:g.46825093A>T | NCBI36 |
| NG_016199.1:g.44171A>T | |
| NG_016199.2:g.44791A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000550257.7:c.2227A>T | ENSP00000447997.3:p.Thr743Ser | |
| ENST00000340802.12:c.2218A>T | ENSP00000345771.6:p.Thr740Ser | |
| ENST00000359794.11:c.2005A>T MANE Select | ENSP00000352842.5:p.Thr669Ser | |
| ENST00000549941.7:c.1747A>T | ENSP00000446829.3:p.Thr583Ser | |
| ENST00000550345.6:c.2005A>T | ENSP00000450369.2:p.Thr669Ser | |
| ENST00000550924.6:c.2005A>T | ENSP00000446945.2:p.Thr669Ser | |
| ENST00000551339.6:c.2005A>T | ENSP00000448253.2:p.Thr669Ser | |
| ENST00000642730.1:c.2314A>T | ENSP00000496597.1:p.Thr772Ser | |
| ENST00000312352.11:c.2005A>T | ENSP00000309438.7:p.Thr669Ser | |
| ENST00000340802.10:c.2218A>T | ENSP00000345771.6:p.Thr740Ser | |
| ENST00000359794.9:c.2005A>T | ENSP00000352842.5:p.Thr669Ser | |
| ENST00000546964.5:n.2329A>T | ||
| ENST00000547581.5:c.*2273A>T | ENSP00000447992.1:n.*2273A>T | |
| ENST00000547587.5:c.2005A>T | ENSP00000449426.1:p.Thr669Ser | |
| ENST00000551804.5:c.1912A>T | ENSP00000448177.1:p.Thr638Ser | |
| ENST00000553055.1:c.281A>T | ||
| NM_000289.5:c.2005A>T | NP_000280.1:p.Thr669Ser | |
| NM_001166686.1:c.2218A>T | NP_001160158.1:p.Thr740Ser | |
| NM_001166687.1:c.2005A>T | NP_001160159.1:p.Thr669Ser | |
| NM_001166688.1:c.2005A>T | NP_001160160.1:p.Thr669Ser | |
| XM_005268974.1:c.2314A>T | XP_005269031.1:p.Thr772Ser | |
| XM_005268975.1:c.2314A>T | XP_005269032.1:p.Thr772Ser | |
| XM_005268976.2:c.2314A>T | XP_005269033.1:p.Thr772Ser | |
| XM_005268977.1:c.2218A>T | XP_005269034.1:p.Thr740Ser | |
| XM_005268978.2:c.2218A>T | XP_005269035.1:p.Thr740Ser | |
| XM_005268979.1:c.2218A>T | XP_005269036.1:p.Thr740Ser | |
| XM_011538487.1:c.2221A>T | XP_011536789.1:p.Thr741Ser | |
| XM_011538488.1:c.2005A>T | XP_011536790.1:p.Thr669Ser | |
| NM_000289.6:c.2005A>T MANE Select | NP_000280.1:p.Thr669Ser | |
| NM_001166686.2:c.2218A>T | NP_001160158.1:p.Thr740Ser | |
| NM_001354735.1:c.2314A>T | NP_001341664.1:p.Thr772Ser | |
| NM_001354736.1:c.2314A>T | NP_001341665.1:p.Thr772Ser | |
| NM_001354737.1:c.2218A>T | NP_001341666.1:p.Thr740Ser | |
| NM_001354738.1:c.2218A>T | NP_001341667.1:p.Thr740Ser | |
| NM_001354739.1:c.2218A>T | NP_001341668.1:p.Thr740Ser | |
| NM_001354740.1:c.2149A>T | NP_001341669.1:p.Thr717Ser | |
| NM_001354741.1:c.2029A>T | NP_001341670.1:p.Thr677Ser | |
| NM_001354742.1:c.2005A>T | NP_001341671.1:p.Thr669Ser | |
| NM_001354743.1:c.2005A>T | NP_001341672.1:p.Thr669Ser | |
| NM_001354744.1:c.2005A>T | NP_001341673.1:p.Thr669Ser | |
| NM_001354745.1:c.1918A>T | NP_001341674.1:p.Thr640Ser | |
| NM_001354746.1:c.1879A>T | NP_001341675.1:p.Thr627Ser | |
| NM_001354747.1:c.1855A>T | NP_001341676.1:p.Thr619Ser | |
| NM_001354748.1:c.1855A>T | NP_001341677.1:p.Thr619Ser | |
| NM_001363619.1:c.1912A>T | NP_001350548.1:p.Thr638Ser | |
| NR_148954.1:n.2442A>T | ||
| NR_148955.1:n.3078A>T | ||
| NR_148956.1:n.2368A>T | ||
| NR_148957.1:n.2597A>T | ||
| NR_148958.1:n.2345A>T | ||
| NR_148959.1:n.2271A>T | ||
| XM_005268976.3:c.2314A>T | XP_005269033.1:p.Thr772Ser | |
| XM_017019469.1:c.2125A>T | XP_016874958.1:p.Thr709Ser | |
| XM_024449020.1:c.2227A>T | XP_024304788.1:p.Thr743Ser | |
| XM_024449021.1:c.2104A>T | XP_024304789.1:p.Thr702Ser | |
| XM_024449022.1:c.2005A>T | XP_024304790.1:p.Thr669Ser | |
| NM_001166687.2:c.2005A>T | NP_001160159.1:p.Thr669Ser | |
| NM_001166688.2:c.2005A>T | NP_001160160.1:p.Thr669Ser | |
| NM_001354741.2:c.2029A>T | NP_001341670.1:p.Thr677Ser | |
| NM_001354742.2:c.2005A>T | NP_001341671.1:p.Thr669Ser | |
| NM_001354743.2:c.2005A>T | NP_001341672.1:p.Thr669Ser | |
| NM_001354744.2:c.2005A>T | NP_001341673.1:p.Thr669Ser | |
| NM_001354745.2:c.1918A>T | NP_001341674.1:p.Thr640Ser | |
| NM_001354746.2:c.1879A>T | NP_001341675.1:p.Thr627Ser | |
| NM_001354747.2:c.1855A>T | NP_001341676.1:p.Thr619Ser | |
| NM_001354748.2:c.1855A>T | NP_001341677.1:p.Thr619Ser | |
| NM_001363619.2:c.1912A>T | NP_001350548.1:p.Thr638Ser | |
| NR_148954.2:n.2308A>T | ||
| NR_148956.2:n.2234A>T | ||
| NR_148957.2:n.2463A>T | ||
| NR_148958.2:n.2211A>T | ||
| NR_148959.2:n.2137A>T |