Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67932030T= , CM000666.2:g.67932030T= | GRCh38 |
| NC_000004.11:g.68797748T= , CM000666.1:g.68797748T= | GRCh37 |
| NC_000004.10:g.68480343T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508048.6:c.283A= MANE Select | ENSP00000426911.2:p.Lys95= | |
| ENST00000334830.11:c.292A= | ENSP00000334611.7:p.Lys98= | |
| ENST00000396188.3:c.283A= | ENSP00000379491.3:p.Lys95= | |
| ENST00000508048.5:c.283A= | ENSP00000426911.2:p.Lys95= | |
| ENST00000513536.5:c.223A= | ENSP00000427621.1:p.Lys75= | |
| NM_001114387.1:c.283A= | NP_001107859.1:p.Lys95= | |
| NM_182606.3:c.292A= | NP_872412.3:p.Lys98= | |
| NM_001114387.2:c.283A= MANE Select | NP_001107859.1:p.Lys95= | |
| NM_182606.4:c.292A= | NP_872412.3:p.Lys98= |