HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659846_31659847insTAAT , CM000683.2:g.31659846_31659847insTAAT | GRCh38 |
NC_000021.8:g.33032159_33032160insTAAT , CM000683.1:g.33032159_33032160insTAAT | GRCh37 |
NC_000021.7:g.31954030_31954031insTAAT | NCBI36 |
NG_008689.1:g.5225_5226insTAAT , LRG_652:g.5225_5226insTAAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.72+5_72+6insTAAT MANE Select | ENSP00000270142.7:n.72+5_72+6insTAAT | |
ENST00000270142.10:c.72+5_72+6insTAAT | ENSP00000270142.6:n.72+5_72+6insTAAT | |
ENST00000389995.4:c.15+62_15+63insTAAT | ENSP00000374645.4:n.15+62_15+63insTAAT | |
ENST00000470944.1:n.138_139insTAAT | ||
ENST00000476106.5:n.149+5_149+6insTAAT | ||
NM_000454.4:c.72+5_72+6insTAAT , LRG_652t1:c.72+5_72+6insTAAT | NP_000445.1:n.72+5_72+6insTAAT | |
NM_000454.5:c.72+5_72+6insTAAT MANE Select | NP_000445.1:n.72+5_72+6insTAAT |