Canonical Allele Identifier:
CA2000590056
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112164907_112164909delinsATT , CM000673.2:g.112164907_112164909delinsATT | GRCh38 |
| NC_000011.9:g.112035630_112035632delinsATT , CM000673.1:g.112035630_112035632delinsATT | GRCh37 |
| NC_000011.8:g.111540840_111540842delinsATT | NCBI36 |
| NG_028143.1:g.4209_4211delinsAAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525987.5:n.320-5512_320-5510delinsATT | ||
| ENST00000531744.5:c.315-5512_315-5510delinsATT | ENSP00000456957.1:n.315-5512_315-5510delinsATT | |
| ENST00000532699.1:c.315-5512_315-5510delinsATT | ENSP00000456434.1:n.315-5512_315-5510delinsATT |