HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33443565del , CM000682.2:g.33443565del | GRCh38 |
NC_000020.10:g.32031371del , CM000682.1:g.32031371del | GRCh37 |
NC_000020.9:g.31495032del | NCBI36 |
NG_011622.1:g.5328del , LRG_332:g.5328del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.56del MANE Select | ENSP00000217381.2:p.Ala19GlyfsTer15 | |
ENST00000217381.2:c.56del | ENSP00000217381.2:p.Ala19GlyfsTer15 | |
NM_003098.2:c.56del , LRG_332t1:c.56del | NP_003089.1:p.Ala19GlyfsTer15 | |
XM_005260517.1:c.56del | XP_005260574.1:p.Ala19GlyfsTer15 | |
XM_011529007.1:c.56del | XP_011527309.1:p.Ala19GlyfsTer15 | |
XM_011529008.1:c.56del | XP_011527310.1:p.Ala19GlyfsTer15 | |
XR_936612.1:n.289del | ||
NM_003098.3:c.56del MANE Select | NP_003089.1:p.Ala19GlyfsTer15 |