HGVS | Genome Assembly |
---|---|
NC_000015.10:g.38253081_38253106del , CM000677.2:g.38253081_38253106del | GRCh38 |
NC_000015.9:g.38545282_38545307del , CM000677.1:g.38545282_38545307del | GRCh37 |
NC_000015.8:g.36332574_36332599del | NCBI36 |
NG_008980.1:g.5231_5256del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299084.9:c.-105_-80del MANE Select | ENSP00000299084.4:n.-105_-80del | |
ENST00000299084.8:c.-105_-80del | ENSP00000299084.4:n.-105_-80del | |
ENST00000561205.1:n.234_259del | ||
NM_152594.2:c.-105_-80del | NP_689807.1:n.-105_-80del | |
XM_005254202.2:c.-105_-80del | XP_005254259.1:n.-105_-80del | |
XM_005254203.3:c.-152_-127del | XP_005254260.1:n.-152_-127del | |
XM_005254202.3:c.-105_-80del | XP_005254259.1:n.-105_-80del | |
XR_001751484.1:n.87+470_87+495del | ||
NM_152594.3:c.-105_-80del MANE Select | NP_689807.1:n.-105_-80del |