HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085716_186085717delinsTC , CM000666.2:g.186085716_186085717delinsTC | GRCh38 |
NC_000004.11:g.187006870_187006871delinsTC , CM000666.1:g.187006870_187006871delinsTC | GRCh37 |
NC_000004.10:g.187243864_187243865delinsTC | NCBI36 |
NG_007278.1:g.21562_21563delinsTC , LRG_117:g.21562_21563delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3110_*3111delinsTC | ENSP00000513675.1:n.*3110_*3111delinsTC | |
ENST00000698353.1:n.3433_3434delinsTC | ||
ENST00000698354.1:c.*843_*844delinsTC | ENSP00000513676.1:n.*843_*844delinsTC | |
ENST00000296795.8:c.*843_*844delinsTC MANE Select | ENSP00000296795.3:n.*843_*844delinsTC | |
ENST00000296795.7:c.*843_*844delinsTC | ENSP00000296795.2:n.*843_*844delinsTC | |
NM_003265.3:c.*843_*844delinsTC MANE Select | NP_003256.1:n.*843_*844delinsTC |