HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1013890_1013891insG , CM000663.2:g.1013890_1013891insG | GRCh38 |
NC_000001.10:g.949270_949271insG , CM000663.1:g.949270_949271insG | GRCh37 |
NC_000001.9:g.939133_939134insG | NCBI36 |
NG_033033.1:g.5424_5425insG | |
NG_033033.2:g.17753_17754insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.-21-94_-21-93insG | ENSP00000485643.1:n.-21-94_-21-93insG | |
ENST00000649529.1:c.4-94_4-93insG MANE Select | ENSP00000496832.1:n.4-94_4-93insG | |
ENST00000379389.4:c.4-94_4-93insG | ENSP00000368699.4:n.4-94_4-93insG | |
ENST00000624652.1:c.-21-94_-21-93insG | ENSP00000485313.1:n.-21-94_-21-93insG | |
ENST00000624697.3:c.-21-94_-21-93insG | ENSP00000485643.1:n.-21-94_-21-93insG | |
NM_005101.3:c.4-94_4-93insG | NP_005092.1:n.4-94_4-93insG | |
NM_005101.4:c.4-94_4-93insG MANE Select | NP_005092.1:n.4-94_4-93insG |