Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104033968dup , CM000672.2:g.104033968dup | GRCh38 |
| NC_000010.10:g.105793726dup , CM000672.1:g.105793726dup | GRCh37 |
| NC_000010.9:g.105783716dup | NCBI36 |
| NG_007069.1:g.56913dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369733.8:c.3887dup | ENSP00000358748.3:p.Arg1297GlufsTer? | |
| ENST00000647647.1:c.163dup | ||
| ENST00000648076.2:c.4133dup MANE Select | ENSP00000497653.1:p.Arg1379GlufsTer? | |
| ENST00000353479.9:c.4133dup | ENSP00000340937.5:p.Arg1379GlufsTer? | |
| ENST00000369733.7:c.3887dup | ENSP00000358748.3:p.Arg1297GlufsTer? | |
| NM_000494.3:c.4133dup | NP_000485.3:p.Arg1379GlufsTer? | |
| NM_000494.4:c.4133dup MANE Select | NP_000485.3:p.Arg1379GlufsTer? |