HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322702_73322719del , CM000677.2:g.73322702_73322719del | GRCh38 |
NC_000015.9:g.73615043_73615060del , CM000677.1:g.73615043_73615060del | GRCh37 |
NC_000015.8:g.71402096_71402113del | NCBI36 |
NG_009063.1:g.51557_51574del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3385_3402del MANE Select | ENSP00000261917.3:p.Ser1129_Gly1134del | |
ENST00000261917.3:c.3385_3402del | ENSP00000261917.3:p.Ser1129_Gly1134del | |
NM_005477.2:c.3385_3402del | NP_005468.1:p.Ser1129_Gly1134del | |
XM_011521148.1:c.2167_2184del | XP_011519450.1:p.Ser723_Gly728del | |
XM_011521148.2:c.2167_2184del | XP_011519450.1:p.Ser723_Gly728del | |
NM_005477.3:c.3385_3402del MANE Select | NP_005468.1:p.Ser1129_Gly1134del |