HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116173544_116173545insA , CM000685.2:g.116173544_116173545insA | GRCh38 |
NC_000023.10:g.115304797_115304798insA , CM000685.1:g.115304797_115304798insA | GRCh37 |
NC_000023.9:g.115218825_115218826insA | NCBI36 |
NG_016326.1:g.7840_7841insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.*172_*173insA MANE Select | ENSP00000360973.4:n.*172_*173insA | |
ENST00000371906.4:c.*172_*173insA | ENSP00000360973.4:n.*172_*173insA | |
NM_000686.4:c.*172_*173insA | NP_000677.2:n.*172_*173insA | |
XM_011537533.1:c.*172_*173insA | XP_011535835.1:n.*172_*173insA | |
NM_000686.5:c.*172_*173insA MANE Select | NP_000677.2:n.*172_*173insA | |
NM_001385624.1:c.*172_*173insA | NP_001372553.1:n.*172_*173insA |