Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648163dup , CM000673.2:g.69648163dup | GRCh38 |
| NC_000011.9:g.69462931dup , CM000673.1:g.69462931dup | GRCh37 |
| NC_000011.8:g.69172112dup | NCBI36 |
| NG_007375.1:g.12059dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.723+21dup MANE Select | ENSP00000227507.2:n.723+21dup | |
| ENST00000227507.2:c.723+21dup | ENSP00000227507.2:n.723+21dup | |
| ENST00000536559.1:c.*164dup | ENSP00000438482.1:n.*164dup | |
| ENST00000542367.1:n.186+21dup | ||
| NM_053056.2:c.723+21dup | NP_444284.1:n.723+21dup | |
| XM_006718653.2:c.747+21dup | XP_006718716.1:n.747+21dup | |
| NM_053056.3:c.723+21dup MANE Select | NP_444284.1:n.723+21dup |