HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370641_34370644delinsGTGA , CM000683.2:g.34370641_34370644delinsGTGA | GRCh38 |
NC_000021.8:g.35742940_35742943delinsGTGA , CM000683.1:g.35742940_35742943delinsGTGA | GRCh37 |
NC_000021.7:g.34664810_34664813delinsGTGA | NCBI36 |
NG_008804.1:g.11618_11621delinsGTGA , LRG_291:g.11618_11621delinsGTGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290310.4:c.163_166delinsGTGA MANE Select | ENSP00000290310.2:p.Val55= | |
ENST00000290310.3:c.163_166delinsGTGA | ENSP00000290310.2:p.Val55= | |
NM_172201.1:c.163_166delinsGTGA , LRG_291t1:c.163_166delinsGTGA | NP_751951.1:p.Val55= | |
XR_937683.1:n.677_680delinsTCAC | ||
XR_937684.1:n.677_680delinsTCAC | ||
XR_001755012.2:n.798_801delinsTCAC | ||
XR_001755013.2:n.677_680delinsTCAC | ||
XR_937683.2:n.677_680delinsTCAC | ||
NM_172201.2:c.163_166delinsGTGA MANE Select | NP_751951.1:p.Val55= |