Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189575171A= , CM000664.2:g.189575171A= | GRCh38 |
| NC_000002.11:g.190439897A= , CM000664.1:g.190439897A= | GRCh37 |
| NC_000002.10:g.190148142A= | NCBI36 |
| NG_009027.1:g.10641T= , LRG_837:g.10641T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261024.7:c.261T= MANE Select | ENSP00000261024.3:p.Ala87= | |
| ENST00000261024.6:c.261T= | ENSP00000261024.2:p.Ala87= | |
| ENST00000418714.1:n.702T= | ||
| ENST00000427241.5:c.261T= | ENSP00000390005.1:p.Ala87= | |
| ENST00000479598.5:n.542T= | ||
| NM_014585.5:c.261T= , LRG_837t1:c.261T= | NP_055400.1:p.Ala87= | |
| XM_005246505.1:c.141T= | XP_005246562.1:p.Ala47= | |
| XM_005246505.2:c.141T= | XP_005246562.1:p.Ala47= | |
| XM_017003938.2:c.141T= | XP_016859427.1:p.Ala47= | |
| NM_014585.6:c.261T= MANE Select | NP_055400.1:p.Ala87= |