HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813747_129813751delinsCTTCT , CM000671.2:g.129813747_129813751delinsCTTCT | GRCh38 |
NC_000009.11:g.132576026_132576030delinsCTTCT , CM000671.1:g.132576026_132576030delinsCTTCT | GRCh37 |
NC_000009.10:g.131615847_131615851delinsCTTCT | NCBI36 |
NG_008049.1:g.15412_15416delinsAGAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*221_*225delinsAGAAG MANE Select | ENSP00000345719.4:n.*221_*225delinsAGAAG | |
ENST00000651202.1:c.*488_*492delinsAGAAG | ENSP00000498222.1:n.*488_*492delinsAGAAG | |
ENST00000351698.4:c.*221_*225delinsAGAAG | ENSP00000345719.4:n.*221_*225delinsAGAAG | |
ENST00000474192.1:n.804_808delinsAGAAG | ||
NM_000113.2:c.*221_*225delinsAGAAG | NP_000104.1:n.*221_*225delinsAGAAG | |
XR_929731.3:n.1415_1419delinsAGAAG | ||
NM_000113.3:c.*221_*225delinsAGAAG MANE Select | NP_000104.1:n.*221_*225delinsAGAAG |