Canonical Allele Identifier:
CA2000590668
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112166613_112166614delinsCT , CM000673.2:g.112166613_112166614delinsCT | GRCh38 |
| NC_000011.9:g.112037336_112037337delinsCT , CM000673.1:g.112037336_112037337delinsCT | GRCh37 |
| NC_000011.8:g.111542546_111542547delinsCT | NCBI36 |
| NG_028143.1:g.2504_2505delinsAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525987.5:n.320-3806_320-3805delinsCT | ||
| ENST00000531744.5:c.315-3806_315-3805delinsCT | ENSP00000456957.1:n.315-3806_315-3805delinsCT | |
| ENST00000532699.1:c.315-3806_315-3805delinsCT | ENSP00000456434.1:n.315-3806_315-3805delinsCT |