HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154957342_154957350del , CM000685.2:g.154957342_154957350del | GRCh38 |
NC_000023.10:g.154185617_154185625del , CM000685.1:g.154185617_154185625del | GRCh37 |
NC_000023.9:g.153838811_153838819del | NCBI36 |
NG_011403.1:g.70374_70382del | |
NG_011403.2:g.70374_70382del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1538-179_1538-171del MANE Select | ENSP00000353393.4:n.1538-179_1538-171del | |
ENST00000647125.1:c.*1414-179_*1414-171del | ENSP00000496062.1:n.*1414-179_*1414-171del | |
ENST00000360256.8:c.1538-179_1538-171del | ENSP00000353393.4:n.1538-179_1538-171del | |
NM_000132.3:c.1538-179_1538-171del | NP_000123.1:n.1538-179_1538-171del | |
XM_011531126.1:c.1433-179_1433-171del | XP_011529428.1:n.1433-179_1433-171del | |
NM_000132.4:c.1538-179_1538-171del MANE Select | NP_000123.1:n.1538-179_1538-171del |