HGVS | Genome Assembly |
---|---|
NC_000015.10:g.90501157_90501158delinsAG , CM000677.2:g.90501157_90501158delinsAG | GRCh38 |
NC_000015.9:g.91044389_91044390delinsAG , CM000677.1:g.91044389_91044390delinsAG | GRCh37 |
NC_000015.8:g.88845393_88845394delinsAG | NCBI36 |
NG_052946.1:g.117917_117918delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000268182.10:c.*1049_*1050delinsAG MANE Select | ENSP00000268182.5:n.*1049_*1050delinsAG | |
ENST00000268182.9:c.*1049_*1050delinsAG | ENSP00000268182.5:n.*1049_*1050delinsAG | |
ENST00000558957.1:n.2081_2082delinsAG | ||
ENST00000561086.1:n.1790_1791delinsAG | ||
NM_003870.3:c.*1049_*1050delinsAG | NP_003861.1:n.*1049_*1050delinsAG | |
XR_001751409.2:n.6152_6153delinsAG | ||
NM_003870.4:c.*1049_*1050delinsAG MANE Select | NP_003861.1:n.*1049_*1050delinsAG |