HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14871699_14871700insT , CM000667.2:g.14871699_14871700insT | GRCh38 |
NC_000005.9:g.14871808_14871809insT , CM000667.1:g.14871808_14871809insT | GRCh37 |
NC_000005.8:g.14924808_14924809insT | NCBI36 |
NG_008273.1:g.5079_5080insA | |
NG_008273.2:g.5086_5087insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284268.8:c.-253_-252insA MANE Select | ENSP00000284268.6:n.-253_-252insA | |
ENST00000284268.6:c.-253_-252insA | ENSP00000284268.6:n.-253_-252insA | |
ENST00000505140.1:c.-253_-252insA | ENSP00000426332.1:n.-253_-252insA | |
NM_054027.4:c.-253_-252insA | NP_473368.1:n.-253_-252insA | |
XM_011514067.1:c.-253_-252insA | XP_011512369.1:n.-253_-252insA | |
NM_054027.5:c.-253_-252insA | NP_473368.1:n.-253_-252insA | |
NM_054027.6:c.-253_-252insA MANE Select | NP_473368.1:n.-253_-252insA |