Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869296dup , CM000664.2:g.240869296dup | GRCh38 |
| NC_000002.11:g.241808713dup , CM000664.1:g.241808713dup | GRCh37 |
| NC_000002.10:g.241457386dup | NCBI36 |
| NG_008005.1:g.5552dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.292dup MANE Select | ENSP00000302620.3:p.Asp98GlyfsTer? | |
| ENST00000307503.3:c.292dup | ENSP00000302620.3:p.Asp98GlyfsTer? | |
| ENST00000472436.1:n.312dup | ||
| NM_000030.2:c.292dup | NP_000021.1:p.Asp98GlyfsTer? | |
| XR_924060.1:n.405+940dup | ||
| NM_000030.3:c.292dup MANE Select | NP_000021.1:p.Asp98GlyfsTer? |