HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33443593_33443594del , CM000682.2:g.33443593_33443594del | GRCh38 |
NC_000020.10:g.32031399_32031400del , CM000682.1:g.32031399_32031400del | GRCh37 |
NC_000020.9:g.31495060_31495061del | NCBI36 |
NG_011622.1:g.5300_5301del , LRG_332:g.5300_5301del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.28_29del MANE Select | ENSP00000217381.2:p.Thr10ArgfsTer? | |
ENST00000217381.2:c.28_29del | ENSP00000217381.2:p.Thr10ArgfsTer? | |
NM_003098.2:c.28_29del , LRG_332t1:c.28_29del | NP_003089.1:p.Thr10ArgfsTer? | |
XM_005260517.1:c.28_29del | XP_005260574.1:p.Thr10ArgfsTer? | |
XM_011529007.1:c.28_29del | XP_011527309.1:p.Thr10ArgfsTer? | |
XM_011529008.1:c.28_29del | XP_011527310.1:p.Thr10ArgfsTer? | |
XR_936612.1:n.261_262del | ||
NM_003098.3:c.28_29del MANE Select | NP_003089.1:p.Thr10ArgfsTer? |