HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33443525_33443526del , CM000682.2:g.33443525_33443526del | GRCh38 |
NC_000020.10:g.32031331_32031332del , CM000682.1:g.32031331_32031332del | GRCh37 |
NC_000020.9:g.31494992_31494993del | NCBI36 |
NG_011622.1:g.5367_5368del , LRG_332:g.5367_5368del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.95_96del MANE Select | ENSP00000217381.2:p.Leu32ProfsTer? | |
ENST00000217381.2:c.95_96del | ENSP00000217381.2:p.Leu32ProfsTer? | |
NM_003098.2:c.95_96del , LRG_332t1:c.95_96del | NP_003089.1:p.Leu32ProfsTer? | |
XM_005260517.1:c.95_96del | XP_005260574.1:p.Leu32ProfsTer? | |
XM_011529007.1:c.95_96del | XP_011527309.1:p.Leu32ProfsTer? | |
XM_011529008.1:c.95_96del | XP_011527310.1:p.Leu32ProfsTer? | |
XR_936612.1:n.328_329del | ||
NM_003098.3:c.95_96del MANE Select | NP_003089.1:p.Leu32ProfsTer? |