HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23422256_23422257insTGGGTCAG , CM000676.2:g.23422256_23422257insTGGGTCAG | GRCh38 |
NC_000014.8:g.23891465_23891466insTGGGTCAG , CM000676.1:g.23891465_23891466insTGGGTCAG | GRCh37 |
NC_000014.7:g.22961305_22961306insTGGGTCAG | NCBI36 |
NG_007884.1:g.18405_18406insCTGACCCA , LRG_384:g.18405_18406insCTGACCCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3168_3169insCTGACCCA MANE Select | ENSP00000347507.3:p.Gly1057LeufsTer6 | |
ENST00000355349.3:c.3168_3169insCTGACCCA | ENSP00000347507.3:p.Gly1057LeufsTer6 | |
NM_000257.3:c.3168_3169insCTGACCCA | NP_000248.2:p.Gly1057LeufsTer6 | |
XR_245686.3:n.3274_3275insCTGACCCA | ||
XM_017021340.1:c.3168_3169insCTGACCCA | XP_016876829.1:p.Gly1057LeufsTer6 | |
NM_000257.4:c.3168_3169insCTGACCCA MANE Select | NP_000248.2:p.Gly1057LeufsTer6 |