Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624214A= , CM000679.2:g.41624214A= | GRCh38 |
| NC_000017.10:g.39780466A= , CM000679.1:g.39780466A= | GRCh37 |
| NC_000017.9:g.37033992A= | NCBI36 |
| NG_008625.1:g.5417T= | |
| NG_009090.2:g.167499T= , LRG_401:g.167499T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000422.3:c.296T= MANE Select | NP_000413.1:p.Leu99= |
| ENST00000311208.13:c.296T= MANE Select | ENSP00000308452.8:p.Leu99= |
| NM_000422.2:c.296T= | NP_000413.1:p.Leu99= |
| ENST00000311208.12:c.296T= | ENSP00000308452.8:p.Leu99= |
| ENST00000463128.5:c.-312-8T= | ENSP00000468672.1:n.-312-8T= |
| ENST00000491673.1:n.362T= | |
| ENST00000493253.5:n.83T= | |
| ENST00000540235.5:c.71+20T= | ENSP00000441751.2:n.71+20T= |
| ENST00000577817.3:c.251T= | ENSP00000467418.1:p.Leu84= |