HGVS | Genome Assembly |
---|---|
NC_000023.11:g.139562221del , CM000685.2:g.139562221del | GRCh38 |
NC_000023.10:g.138644380del , CM000685.1:g.138644380del | GRCh37 |
NC_000023.9:g.138472046del | NCBI36 |
NG_007994.1:g.36486del , LRG_556:g.36486del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218099.7:c.*150del MANE Select | ENSP00000218099.2:n.*150del | |
ENST00000643157.1:n.1723+480del | ||
ENST00000218099.6:c.*150del | ENSP00000218099.2:n.*150del | |
NM_000133.3:c.*150del , LRG_556t1:c.*150del | NP_000124.1:n.*150del | |
NM_001313913.1:c.*150del | NP_001300842.1:n.*150del | |
XM_005262397.3:c.*150del | XP_005262454.1:n.*150del | |
XM_005262397.4:c.*150del | XP_005262454.1:n.*150del | |
NM_000133.4:c.*150del MANE Select | NP_000124.1:n.*150del | |
NM_001313913.2:c.*150del | NP_001300842.1:n.*150del |