HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6058124_6058125insAAAAAA , CM000674.2:g.6058124_6058125insAAAAAA | GRCh38 |
NC_000012.11:g.6167290_6167291insAAAAAA , CM000674.1:g.6167290_6167291insAAAAAA | GRCh37 |
NC_000012.10:g.6037551_6037552insAAAAAA | NCBI36 |
NG_009072.1:g.71548_71549insTTTTTT | |
NG_009072.2:g.71548_71549insTTTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.1534-79_1534-78insTTTTTT MANE Select | ENSP00000261405.5:n.1534-79_1534-78insTTTTTT | |
ENST00000261405.9:c.1534-79_1534-78insTTTTTT | ENSP00000261405.5:n.1534-79_1534-78insTTTTTT | |
ENST00000538635.5:n.420+52392_420+52393insTTTTTT | ||
NM_000552.3:c.1534-79_1534-78insTTTTTT | NP_000543.2:n.1534-79_1534-78insTTTTTT | |
NM_000552.4:c.1534-79_1534-78insTTTTTT | NP_000543.2:n.1534-79_1534-78insTTTTTT | |
NM_000552.5:c.1534-79_1534-78insTTTTTT MANE Select | NP_000543.3:n.1534-79_1534-78insTTTTTT |