Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94401386_94401388delinsCAT , CM000669.2:g.94401386_94401388delinsCAT | GRCh38 |
| NC_000007.13:g.94030698_94030700delinsCAT , CM000669.1:g.94030698_94030700delinsCAT | GRCh37 |
| NC_000007.12:g.93868634_93868636delinsCAT | NCBI36 |
| NG_007405.1:g.11826_11828delinsCAT , LRG_2:g.11826_11828delinsCAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.226-181_226-179delinsCAT MANE Select | ENSP00000297268.6:n.226-181_226-179delinsCAT | |
| ENST00000297268.10:c.226-181_226-179delinsCAT | ENSP00000297268.6:n.226-181_226-179delinsCAT | |
| ENST00000620463.1:c.220-181_220-179delinsCAT | ENSP00000477719.1:n.220-181_220-179delinsCAT | |
| NM_000089.3:c.226-181_226-179delinsCAT , LRG_2t1:c.226-181_226-179delinsCAT | NP_000080.2:n.226-181_226-179delinsCAT | |
| NM_000089.4:c.226-181_226-179delinsCAT MANE Select | NP_000080.2:n.226-181_226-179delinsCAT |