HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94030874_94030875insAGGAA , CM000663.2:g.94030874_94030875insAGGAA | GRCh38 |
NC_000001.10:g.94496430_94496431insAGGAA , CM000663.1:g.94496430_94496431insAGGAA | GRCh37 |
NC_000001.9:g.94269018_94269019insAGGAA | NCBI36 |
NG_009073.1:g.95275_95276insTTCCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.4253+121_4253+122insTTCCT MANE Select | ENSP00000359245.3:n.4253+121_4253+122insT... | |
ENST00000370225.3:c.4253+121_4253+122insTTCCT | ENSP00000359245.3:n.4253+121_4253+122insT... | |
ENST00000536513.5:c.629+121_629+122insTTCCT | ENSP00000439707.2:n.629+121_629+122insTTC... | |
NM_000350.2:c.4253+121_4253+122insTTCCT | NP_000341.2:n.4253+121_4253+122insTTCCT | |
NM_000350.3:c.4253+121_4253+122insTTCCT MANE Select | NP_000341.2:n.4253+121_4253+122insTTCCT |