HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202806_32202807insCTTGC , CM000668.2:g.32202806_32202807insCTTGC | GRCh38 |
NC_000006.11:g.32170583_32170584insCTTGC , CM000668.1:g.32170583_32170584insCTTGC | GRCh37 |
NC_000006.10:g.32278561_32278562insCTTGC | NCBI36 |
NG_028190.1:g.26261_26262insGCAAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-208_3232-207insGCAAG MANE Select | ENSP00000364163.3:n.3232-208_3232-207insGCAAG | |
ENST00000474612.1:n.1110_1111insGCAAG | ||
NM_004557.3:c.3232-208_3232-207insGCAAG | NP_004548.3:n.3232-208_3232-207insGCAAG | |
NR_134949.1:n.3472+963_3472+964insGCAAG | ||
NR_134950.1:n.3370+963_3370+964insGCAAG | ||
NM_004557.4:c.3232-208_3232-207insGCAAG MANE Select | NP_004548.3:n.3232-208_3232-207insGCAAG | |
NR_134949.2:n.3472+963_3472+964insGCAAG | ||
NR_134950.2:n.3370+963_3370+964insGCAAG |