Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92616744T= , CM000672.2:g.92616744T= | GRCh38 |
| NC_000010.10:g.94376501T= , CM000672.1:g.94376501T= | GRCh37 |
| NC_000010.9:g.94366481T= | NCBI36 |
| NG_032580.1:g.28677T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004523.4:c.1040T= MANE Select | NP_004514.2:p.Leu347= |
| ENST00000260731.5:c.1040T= MANE Select | ENSP00000260731.3:p.Leu347= |
| NM_004523.3:c.1040T= | NP_004514.2:p.Leu347= |
| ENST00000260731.4:c.1040T= | ENSP00000260731.3:p.Leu347= |
| ENST00000676621.1:c.1040T= | ENSP00000503639.1:p.Leu347= |
| ENST00000676647.1:c.833T= | ENSP00000503394.1:p.Leu278= |
| ENST00000676757.1:c.833T= | ENSP00000504289.1:p.Leu278= |
| ENST00000677720.1:c.1040T= | ENSP00000504840.1:p.Leu347= |