Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55157589T= , CM000681.2:g.55157589T= | GRCh38 |
| NC_000019.9:g.55668957T= , CM000681.1:g.55668957T= | GRCh37 |
| NC_000019.8:g.60360769T= | NCBI36 |
| NG_007866.2:g.5144A= , LRG_432:g.5144A= | |
| NG_032759.1:g.14134A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.1A= MANE Select | NP_000354.4:p.Met1= |
| ENST00000344887.10:c.1A= MANE Select | ENSP00000341838.5:p.Met1= |
| NM_000363.4:c.1A= , LRG_432t1:c.1A= | NP_000354.4:p.Met1= |
| ENST00000344887.9:c.1A= | ENSP00000341838.5:p.Met1= |
| ENST00000586446.1:n.144A= | |
| ENST00000587176.5:n.185A= | |
| ENST00000587871.1:c.621A= | |
| ENST00000590463.1:n.128A= | |
| ENST00000665070.1:c.1A= | ENSP00000499482.1:p.Met1= |