HGVS | Genome Assembly |
---|---|
NC_000007.14:g.151187314_151187328del , CM000669.2:g.151187314_151187328del | GRCh38 |
NC_000007.13:g.150884401_150884415del , CM000669.1:g.150884401_150884415del | GRCh37 |
NC_000007.12:g.150515334_150515348del | NCBI36 |
NG_017016.1:g.5506_5520del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000275838.5:c.-197_-183del | ENSP00000275838.1:n.-197_-183del | |
ENST00000377867.7:c.271+125_271+139del | ENSP00000367098.3:n.271+125_271+139del | |
ENST00000415615.1:c.*48_*62del | ENSP00000410871.1:n.*48_*62del | |
NM_001142459.1:c.-197_-183del | NP_001135931.2:n.-197_-183del | |
NM_001142460.1:c.-197_-183del | NP_001135932.2:n.-197_-183del | |
NM_080871.3:c.271+125_271+139del | NP_543147.2:n.271+125_271+139del | |
NM_080871.4:c.271+125_271+139del | NP_543147.2:n.271+125_271+139del |