HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213387_1213388insTT , CM000667.2:g.1213387_1213388insTT | GRCh38 |
NC_000005.9:g.1213502_1213503insTT , CM000667.1:g.1213502_1213503insTT | GRCh37 |
NC_000005.8:g.1266502_1266503insTT | NCBI36 |
NG_008282.1:g.16793_16794insTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-76_664-75insTT MANE Select | ENSP00000305302.10:n.664-76_664-75insTT | |
ENST00000304460.10:c.664-76_664-75insTT | ENSP00000305302.10:n.664-76_664-75insTT | |
ENST00000515652.5:c.572-76_572-75insTT | ENSP00000425701.1:n.572-76_572-75insTT | |
NM_001003841.2:c.664-76_664-75insTT | NP_001003841.1:n.664-76_664-75insTT | |
NM_001003841.3:c.664-76_664-75insTT MANE Select | NP_001003841.1:n.664-76_664-75insTT |