Revel Score:
ENST00000269228 (MANE Select)
0.358
ENST00000412552
0.358
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.23538651G>T , CM000680.2:g.23538651G>T | GRCh38 |
| NC_000018.9:g.21118615G>T , CM000680.1:g.21118615G>T | GRCh37 |
| NC_000018.8:g.19372613G>T | NCBI36 |
| NG_012795.1:g.52967C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269228.10:c.2932C>A MANE Select | ENSP00000269228.4:p.Arg978Ser | |
| ENST00000269228.9:c.2932C>A | ENSP00000269228.4:p.Arg978Ser | |
| ENST00000591051.1:c.2010C>A | ||
| ENST00000591075.1:n.565C>A | ||
| ENST00000591955.1:n.275C>A | ||
| NM_000271.4:c.2932C>A | NP_000262.2:p.Arg978Ser | |
| XM_005258277.1:c.2983C>A | XP_005258334.1:p.Arg995Ser | |
| XM_005258278.3:c.2983C>A | XP_005258335.1:p.Arg995Ser | |
| XM_005258279.1:c.2932C>A | XP_005258336.1:p.Arg978Ser | |
| XM_006722479.2:c.2983C>A | XP_006722542.1:p.Arg995Ser | |
| XM_011526015.1:c.2518C>A | XP_011524317.1:p.Arg840Ser | |
| XM_005258278.5:c.2983C>A | XP_005258335.1:p.Arg995Ser | |
| XM_005258279.2:c.2932C>A | XP_005258336.1:p.Arg978Ser | |
| XM_006722479.3:c.2983C>A | XP_006722542.1:p.Arg995Ser | |
| XM_017025784.1:c.2983C>A | XP_016881273.1:p.Arg995Ser | |
| XM_017025785.1:c.2983C>A | XP_016881274.1:p.Arg995Ser | |
| XM_017025786.1:c.2932C>A | XP_016881275.1:p.Arg978Ser | |
| XM_017025787.1:c.2932C>A | XP_016881276.1:p.Arg978Ser | |
| NM_000271.5:c.2932C>A MANE Select | NP_000262.2:p.Arg978Ser |