HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29945977_29945981delinsTGCTT , CM000668.2:g.29945977_29945981delinsTGCTT | GRCh38 |
NC_000006.11:g.29913754_29913758delinsTGCTT , CM000668.1:g.29913754_29913758delinsTGCTT | GRCh37 |
NC_000006.10:g.30021733_30021737delinsTGCTT | NCBI36 |
NG_029217.2:g.8513_8517delinsTGCTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706901.1:c.*522_*526delinsTGCTT | ENSP00000516612.1:n.*522_*526delinsTGCTT | |
ENST00000706902.1:c.1093+696_1093+700delinsTGCTT | ENSP00000516613.1:n.1093+696_1093+700delinsTGCTT | |
ENST00000706903.1:c.*124+398_*124+402delinsTGCTT | ENSP00000516614.1:n.*124+398_*124+402delinsTGCTT | |
ENST00000706904.1:c.1093+696_1093+700delinsTGCTT | ENSP00000516615.1:n.1093+696_1093+700delinsTGCTT | |
ENST00000706905.1:c.*522_*526delinsTGCTT | ENSP00000516616.1:n.*522_*526delinsTGCTT |