Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14141746T= , CM000665.2:g.14141746T= | GRCh38 |
| NC_000003.11:g.14183246T= , CM000665.1:g.14183246T= | GRCh37 |
| NC_000003.10:g.14158247T= | NCBI36 |
| NG_008975.1:g.21807T= , LRG_435:g.21807T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024334.3:c.1154T= MANE Select | NP_077310.1:p.Val385= |
| ENST00000306077.5:c.1154T= MANE Select | ENSP00000303992.5:p.Val385= |
| NM_024334.2:c.1154T= , LRG_435t1:c.1154T= | NP_077310.1:p.Val385= |
| ENST00000306077.4:c.1154T= | ENSP00000303992.4:p.Val385= |
| ENST00000432444.2:c.*1184T= | ENSP00000395617.1:n.*1184T= |
| ENST00000601399.3:n.327+2449T= | |
| ENST00000608606.1:c.236+2449T= | |
| ENST00000626721.1:n.19T= | |
| XM_011534109.1:c.1049T= | XP_011532411.1:p.Val350= |
| XM_017007176.2:c.1049T= | XP_016862665.1:p.Val350= |