Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6022179_6022180insGC , CM000674.2:g.6022179_6022180insGC | GRCh38 |
| NC_000012.11:g.6131345_6131346insGC , CM000674.1:g.6131345_6131346insGC | GRCh37 |
| NC_000012.10:g.6001606_6001607insGC | NCBI36 |
| NG_009072.1:g.107491_107492insGC | |
| NG_009072.2:g.107491_107492insGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.3539-145_3539-144insGC MANE Select | ENSP00000261405.5:n.3539-145_3539-144insGC | |
| ENST00000261405.9:c.3539-145_3539-144insGC | ENSP00000261405.5:n.3539-145_3539-144insGC | |
| ENST00000538635.5:n.421-28246_421-28245insGC | ||
| NM_000552.3:c.3539-145_3539-144insGC | NP_000543.2:n.3539-145_3539-144insGC | |
| NM_000552.4:c.3539-145_3539-144insGC | NP_000543.2:n.3539-145_3539-144insGC | |
| NM_000552.5:c.3539-145_3539-144insGC MANE Select | NP_000543.3:n.3539-145_3539-144insGC |