dbSNP:
Revel Score:
ENST00000288135 (MANE Select)
0.861
ENST00000412167
0.861
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54736528G>C , CM000666.2:g.54736528G>C | GRCh38 |
| NC_000004.11:g.55602694G>C , CM000666.1:g.55602694G>C | GRCh37 |
| NC_000004.10:g.55297451G>C | NCBI36 |
| NG_007456.1:g.83534G>C , LRG_307:g.83534G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412167.7:c.2503G>C | ENSP00000390987.3:p.Glu835Gln | |
| ENST00000684818.1:n.1207G>C | ||
| ENST00000685269.1:n.2593G>C | ||
| ENST00000686011.1:c.2500G>C | ENSP00000509704.1:p.Glu834Gln | |
| ENST00000687109.1:c.2518G>C | ENSP00000509371.1:p.Glu840Gln | |
| ENST00000687208.1:n.2927G>C | ||
| ENST00000687246.1:c.2380G>C | ENSP00000509114.1:p.Glu794Gln | |
| ENST00000687265.1:n.2673G>C | ||
| ENST00000687295.1:c.2503G>C | ENSP00000509450.1:p.Glu835Gln | |
| ENST00000688060.1:n.312G>C | ||
| ENST00000689832.1:c.2515G>C | ENSP00000509084.1:p.Glu839Gln | |
| ENST00000689994.1:c.2005G>C | ENSP00000509156.1:p.Glu669Gln | |
| ENST00000690543.1:c.2506G>C | ENSP00000508831.1:p.Glu836Gln | |
| ENST00000690917.1:n.2733G>C | ||
| ENST00000691361.1:n.1425G>C | ||
| ENST00000692301.1:n.1207G>C | ||
| ENST00000692783.1:c.2512G>C | ENSP00000508733.1:p.Glu838Gln | |
| ENST00000692991.1:n.2612G>C | ||
| ENST00000288135.6:c.2515G>C MANE Select | ENSP00000288135.6:p.Glu839Gln | |
| ENST00000288135.5:c.2515G>C | ENSP00000288135.5:p.Glu839Gln | |
| ENST00000412167.6:c.2503G>C | ENSP00000390987.2:p.Glu835Gln | |
| NM_000222.2:c.2515G>C , LRG_307t1:c.2515G>C | NP_000213.1:p.Glu839Gln | |
| NM_001093772.1:c.2503G>C | NP_001087241.1:p.Glu835Gln | |
| XM_005265740.1:c.2518G>C | XP_005265797.1:p.Glu840Gln | |
| XM_005265741.1:c.2515G>C | XP_005265798.1:p.Glu839Gln | |
| XM_005265742.1:c.2506G>C | XP_005265799.1:p.Glu836Gln | |
| XM_005265742.3:c.2506G>C | XP_005265799.1:p.Glu836Gln | |
| XM_017008178.1:c.2512G>C | XP_016863667.1:p.Glu838Gln | |
| XM_017008179.1:c.2503G>C | XP_016863668.1:p.Glu835Gln | |
| XM_017008180.1:c.2500G>C | XP_016863669.1:p.Glu834Gln | |
| NM_000222.3:c.2515G>C MANE Select | NP_000213.1:p.Glu839Gln | |
| NM_001093772.2:c.2503G>C | NP_001087241.1:p.Glu835Gln | |
| NM_001385284.1:c.2518G>C | NP_001372213.1:p.Glu840Gln | |
| NM_001385285.1:c.2512G>C | NP_001372214.1:p.Glu838Gln | |
| NM_001385286.1:c.2500G>C | NP_001372215.1:p.Glu834Gln | |
| NM_001385288.1:c.2506G>C | NP_001372217.1:p.Glu836Gln | |
| NM_001385290.1:c.2515G>C | NP_001372219.1:p.Glu839Gln | |
| NM_001385292.1:c.2503G>C | NP_001372221.1:p.Glu835Gln |