HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56450101_56450102insC , CM000674.2:g.56450101_56450102insC | GRCh38 |
NC_000012.11:g.56843885_56843886insC , CM000674.1:g.56843885_56843886insC | GRCh37 |
NC_000012.10:g.55130152_55130153insC | NCBI36 |
NG_021397.1:g.9550_9551insG | |
NG_021397.2:g.24065_24066insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648304.1:c.*1594_*1595insG | ENSP00000497190.1:n.*1594_*1595insG | |
ENST00000652304.1:c.*1178_*1179insG MANE Select | ENSP00000498622.1:n.*1178_*1179insG | |
ENST00000257979.4:c.*1178_*1179insG | ENSP00000257979.4:n.*1178_*1179insG | |
NM_012064.3:c.*1178_*1179insG | NP_036196.1:n.*1178_*1179insG | |
XM_011538354.1:c.*1178_*1179insG | XP_011536656.1:n.*1178_*1179insG | |
NM_012064.4:c.*1178_*1179insG MANE Select | NP_036196.1:n.*1178_*1179insG | |
XM_017019306.1:c.*1178_*1179insG | XP_016874795.1:n.*1178_*1179insG |