Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372388T= , CM000679.2:g.44372388T= | GRCh38 |
| NC_000017.10:g.42449756T= , CM000679.1:g.42449756T= | GRCh37 |
| NC_000017.9:g.39805282T= | NCBI36 |
| NG_008331.1:g.22118A= , LRG_479:g.22118A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3096A= MANE Select | ENSP00000262407.5:p.Glu1032= | |
| ENST00000648408.1:c.2410A= | ||
| ENST00000262407.5:c.3096A= | ENSP00000262407.5:p.Glu1032= | |
| ENST00000587295.5:c.289A= | ||
| ENST00000588098.1:c.73A= | ||
| NM_000419.3:c.3096A= , LRG_479t1:c.3096A= | NP_000410.2:p.Glu1032= | |
| XM_011524749.1:c.2994A= | XP_011523051.1:p.Glu998= | |
| XM_011524750.1:c.2979A= | XP_011523052.1:p.Glu993= | |
| NM_000419.4:c.3096A= | NP_000410.2:p.Glu1032= | |
| NM_000419.5:c.3096A= MANE Select | NP_000410.2:p.Glu1032= |