HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149981937_149981938insTAT , CM000667.2:g.149981937_149981938insTAT | GRCh38 |
NC_000005.9:g.149361500_149361501insTAT , CM000667.1:g.149361500_149361501insTAT | GRCh37 |
NC_000005.8:g.149341693_149341694insTAT | NCBI36 |
NG_007147.2:g.23055_23056insTAT , LRG_684:g.23055_23056insTAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.*124_*125insTAT MANE Select | ENSP00000286298.4:n.*124_*125insTAT | |
ENST00000286298.4:c.*124_*125insTAT | ENSP00000286298.4:n.*124_*125insTAT | |
ENST00000503336.1:c.372+3586_372+3587insTAT | ENSP00000426053.1:n.372+3586_372+3587insTAT | |
NM_000112.3:c.*124_*125insTAT , LRG_684t1:c.*124_*125insTAT | NP_000103.2:n.*124_*125insTAT | |
XM_017009191.2:c.*21_*22insTAT | XP_016864680.1:n.*21_*22insTAT | |
NM_000112.4:c.*124_*125insTAT MANE Select | NP_000103.2:n.*124_*125insTAT |