Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.13884863_13884878delinsATGGCCCCTTTCATGT , CM000680.2:g.13884863_13884878delinsATGGCCCCTTTCATGT | GRCh38 |
| NC_000018.9:g.13884862_13884877delinsATGGCCCCTTTCATGT , CM000680.1:g.13884862_13884877delinsATGGCCCCTTTCATGT | GRCh37 |
| NC_000018.8:g.13874862_13874877delinsATGGCCCCTTTCATGT | NCBI36 |
| NG_011819.1:g.35659_35674delinsACATGAAAGGGGCCAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327606.4:c.641_656delinsACATGAAAGGGGCCAT MANE Select | ENSP00000333821.2:p.Asn214= | |
| ENST00000327606.3:c.641_656delinsACATGAAAGGGGCCAT | ENSP00000333821.2:p.Asn214= | |
| NM_000529.2:c.641_656delinsACATGAAAGGGGCCAT MANE Select | NP_000520.1:p.Asn214= | |
| NM_001291911.1:c.641_656delinsACATGAAAGGGGCCAT | NP_001278840.1:p.Asn214= | |
| XM_017025781.1:c.641_656delinsACATGAAAGGGGCCAT | XP_016881270.1:p.Asn214= |