HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862686_4862687insTTTTTTTTTTTTTTTTCTT , CM000666.2:g.4862686_4862687insTTTTTTTTTTTTTTTTCTT | GRCh38 |
NC_000004.11:g.4864413_4864414insTTTTTTTTTTTTTTTTCTT , CM000666.1:g.4864413_4864414insTTTTTTTTTTTTTTTTCTT | GRCh37 |
NC_000004.10:g.4915314_4915315insTTTTTTTTTTTTTTTTCTT | NCBI36 |
NG_008121.1:g.8022_8023insTTTTTTTTTTTTTTTTCTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-15_470-14insTTTTTTTTTTTTTTTTCTT MANE Select | ENSP00000372170.4:n.470-15_470-14insTTTTTTTTTTTTTTTTCTT | |
ENST00000382723.4:c.470-15_470-14insTTTTTTTTTTTTTTTTCTT | ENSP00000372170.4:n.470-15_470-14insTTTTTTTTTTTTTTTTCTT | |
ENST00000468421.1:n.182-15_182-14insTTTTTTTTTTTTTTTTCTT | ||
NM_002448.3:c.470-15_470-14insTTTTTTTTTTTTTTTTCTT MANE Select | NP_002439.2:n.470-15_470-14insTTTTTTTTTTTTTTTTCTT |