HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003834_47003835insTAAAAAA , CM000681.2:g.47003834_47003835insTAAAAAA | GRCh38 |
NC_000019.9:g.47507091_47507092insTAAAAAA , CM000681.1:g.47507091_47507092insTAAAAAA | GRCh37 |
NC_000019.8:g.52198931_52198932insTAAAAAA | NCBI36 |
NG_047014.1:g.90268_90269insTAAAAAA | |
NG_047014.2:g.147838_147839insTAAAAAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7646_7647insTAAAAAA | ENSP00000385720.2:n.7646_7647insTAAAAAA | |
ENST00000672722.1:c.*3146_*3147insTAAAAAA MANE Select | ENSP00000500409.1:n.*3146_*3147insTAAAAAA | |
ENST00000404338.7:c.7646_7647insTAAAAAA | ENSP00000385720.2:n.7646_7647insTAAAAAA | |
ENST00000614079.1:c.7223_7224insTAAAAAA | ENSP00000483730.1:n.7223_7224insTAAAAAA | |
NM_004491.4:c.7646_7647insTAAAAAA | NP_004482.4:n.7646_7647insTAAAAAA | |
NM_004491.5:c.*3146_*3147insTAAAAAA MANE Select | NP_004482.4:n.*3146_*3147insTAAAAAA |