Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154797T= , CM000681.2:g.55154797T= | GRCh38 |
| NC_000019.9:g.55666165T= , CM000681.1:g.55666165T= | GRCh37 |
| NC_000019.8:g.60357977T= | NCBI36 |
| NG_007866.2:g.7936A= , LRG_432:g.7936A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.316A= MANE Select | ENSP00000341838.5:p.Lys106= | |
| ENST00000665070.1:c.316A= | ENSP00000499482.1:p.Lys106= | |
| ENST00000344887.9:c.316A= | ENSP00000341838.5:p.Lys106= | |
| ENST00000585806.5:n.315A= | ||
| ENST00000586669.5:n.324A= | ||
| ENST00000587176.5:n.500A= | ||
| ENST00000587871.1:c.935A= | ||
| ENST00000588882.1:c.241A= | ENSP00000466729.1:p.Lys81= | |
| ENST00000590463.1:n.488A= | ||
| NM_000363.4:c.316A= , LRG_432t1:c.316A= | NP_000354.4:p.Lys106= | |
| NM_000363.5:c.316A= MANE Select | NP_000354.4:p.Lys106= |