HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73329759_73329760insAG , CM000677.2:g.73329759_73329760insAG | GRCh38 |
NC_000015.9:g.73622100_73622101insAG , CM000677.1:g.73622100_73622101insAG | GRCh37 |
NC_000015.8:g.71409153_71409154insAG | NCBI36 |
NG_009063.1:g.44505_44506insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.1403_1404insCT MANE Select | ENSP00000261917.3:p.Leu469CysfsTer6 | |
ENST00000261917.3:c.1403_1404insCT | ENSP00000261917.3:p.Leu469CysfsTer6 | |
NM_005477.2:c.1403_1404insCT | NP_005468.1:p.Leu469CysfsTer6 | |
XM_011521148.1:c.185_186insCT | XP_011519450.1:p.Leu63CysfsTer6 | |
XM_011521148.2:c.185_186insCT | XP_011519450.1:p.Leu63CysfsTer6 | |
NM_005477.3:c.1403_1404insCT MANE Select | NP_005468.1:p.Leu469CysfsTer6 |