HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70177209_70177210insTTTTCAGT , CM000679.2:g.70177209_70177210insTTTTCAGT | GRCh38 |
NC_000017.10:g.68173350_68173351insTTTTCAGT , CM000679.1:g.68173350_68173351insTTTTCAGT | GRCh37 |
NC_000017.9:g.65684945_65684946insTTTTCAGT | NCBI36 |
NG_008798.1:g.12675_12676insTTTTCAGT , LRG_328:g.12675_12676insTTTTCAGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000243457.4:c.*886_*887insTTTTCAGT MANE Select | ENSP00000243457.2:n.*886_*887insTTTTCAGT | |
ENST00000243457.3:c.*886_*887insTTTTCAGT | ENSP00000243457.2:n.*886_*887insTTTTCAGT | |
NM_000891.2:c.*886_*887insTTTTCAGT , LRG_328t1:c.*886_*887insTTTTCAGT | NP_000882.1:n.*886_*887insTTTTCAGT | |
XM_011524779.1:c.*886_*887insTTTTCAGT | XP_011523081.1:n.*886_*887insTTTTCAGT | |
NM_000891.3:c.*886_*887insTTTTCAGT MANE Select | NP_000882.1:n.*886_*887insTTTTCAGT |