Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99845781A= , CM000672.2:g.99845781A= | GRCh38 |
| NC_000010.10:g.101605538A= , CM000672.1:g.101605538A= | GRCh37 |
| NC_000010.9:g.101595528A= | NCBI36 |
| NG_011798.1:g.68076A= | |
| NG_011798.2:g.68184A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000392.5:c.4145A= MANE Select | NP_000383.2:p.Gln1382= |
| ENST00000647814.1:c.4145A= MANE Select | ENSP00000497274.1:p.Gln1382= |
| NM_000392.4:c.4145A= | NP_000383.1:p.Gln1382= |
| ENST00000370449.8:c.4145A= | ENSP00000359478.4:p.Gln1382= |
| ENST00000648523.1:c.33A= | |
| ENST00000649459.1:n.493A= | |
| XM_006717630.2:c.3449A= | XP_006717693.1:p.Gln1150= |
| XM_006717630.3:c.3449A= | XP_006717693.1:p.Gln1150= |
| XR_945604.1:n.4275A= | |
| XR_945604.3:n.4329A= | |
| XR_945605.1:n.4209A= | |
| XR_945605.3:n.4261A= |