HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652511_171652512insAGCTC , CM000663.2:g.171652511_171652512insAGCTC | GRCh38 |
NC_000001.10:g.171621651_171621652insAGCTC , CM000663.1:g.171621651_171621652insAGCTC | GRCh37 |
NC_000001.9:g.169888274_169888275insAGCTC | NCBI36 |
NG_008859.1:g.5122_5123insGAGCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.100_101insGAGCT MANE Select | ENSP00000037502.5:p.Thr34ArgfsTer? | |
ENST00000638471.1:c.100_101insGAGCT | ENSP00000491206.1:p.Thr34ArgfsTer? | |
ENST00000037502.10:c.100_101insGAGCT | ENSP00000037502.5:p.Thr34ArgfsTer? | |
ENST00000614688.1:c.100_101insGAGCT | ENSP00000478680.1:p.Thr34ArgfsTer? | |
NM_000261.1:c.100_101insGAGCT | NP_000252.1:p.Thr34ArgfsTer? | |
NM_000261.2:c.100_101insGAGCT MANE Select | NP_000252.1:p.Thr34ArgfsTer? |