Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190693_204190714delinsAGGTCCCCCGACGGCTCAGCCT , CM000663.2:g.204190693_204190714delinsAGGTCCCCCGACGGCTCAGCCT | GRCh38 |
| NC_000001.10:g.204159821_204159842delinsAGGTCCCCCGACGGCTCAGCCT , CM000663.1:g.204159821_204159842delinsAGGTCCCCCGACGGCTCAGCCT | GRCh37 |
| NC_000001.9:g.202426444_202426465delinsAGGTCCCCCGACGGCTCAGCCT | NCBI36 |
| NG_032151.1:g.10778_10799delinsAGGCTGAGCCGTCGGGGGACCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.187_208delinsAGGCTGAGCCGTCGGGGGACCT MANE Select | ENSP00000356162.4:p.Arg63= | |
| ENST00000367194.4:c.187_208delinsAGGCTGAGCCGTCGGGGGACCT | ENSP00000356162.4:p.Arg63= | |
| ENST00000625357.1:c.187_208delinsAGGCTGAGCCGTCGGGGGACCT | ENSP00000485957.1:p.Arg63= | |
| NM_002256.3:c.187_208delinsAGGCTGAGCCGTCGGGGGACCT | NP_002247.3:p.Arg63= | |
| XM_011509525.1:c.187_208delinsAGGCTGAGCCGTCGGGGGACCT | XP_011507827.1:p.Arg63= | |
| NM_002256.4:c.187_208delinsAGGCTGAGCCGTCGGGGGACCT MANE Select | NP_002247.3:p.Arg63= |