Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624087C= , CM000679.2:g.41624087C= | GRCh38 |
| NC_000017.10:g.39780339C= , CM000679.1:g.39780339C= | GRCh37 |
| NC_000017.9:g.37033865C= | NCBI36 |
| NG_008625.1:g.5544G= | |
| NG_009090.2:g.167626G= , LRG_401:g.167626G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.423G= MANE Select | ENSP00000308452.8:p.Leu141= | |
| ENST00000311208.12:c.423G= | ENSP00000308452.8:p.Leu141= | |
| ENST00000463128.5:c.-193G= | ENSP00000468672.1:n.-193G= | |
| ENST00000491673.1:n.489G= | ||
| ENST00000493253.5:n.210G= | ||
| ENST00000540235.5:c.174G= | ENSP00000441751.2:p.Leu58= | |
| ENST00000577817.3:c.378G= | ENSP00000467418.1:p.Leu126= | |
| NM_000422.2:c.423G= | NP_000413.1:p.Leu141= | |
| NM_000422.3:c.423G= MANE Select | NP_000413.1:p.Leu141= |