HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94015678_94015682delinsCCCCC , CM000663.2:g.94015678_94015682delinsCCCCC | GRCh38 |
NC_000001.10:g.94481234_94481238delinsCCCCC , CM000663.1:g.94481234_94481238delinsCCCCC | GRCh37 |
NC_000001.9:g.94253822_94253826delinsCCCCC | NCBI36 |
NG_009073.1:g.110468_110472delinsGGGGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.5312+57_5312+61delinsGGGGG MANE Select | ENSP00000359245.3:n.5312+57_5312+61delins... | |
ENST00000370225.3:c.5312+57_5312+61delinsGGGGG | ENSP00000359245.3:n.5312+57_5312+61delins... | |
ENST00000536513.5:c.1688+57_1688+61delinsGGGGG | ENSP00000439707.2:n.1688+57_1688+61delins... | |
NM_000350.2:c.5312+57_5312+61delinsGGGGG | NP_000341.2:n.5312+57_5312+61delinsGGGGG | |
NM_000350.3:c.5312+57_5312+61delinsGGGGG MANE Select | NP_000341.2:n.5312+57_5312+61delinsGGGGG |