HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202687_32202688delinsAG , CM000668.2:g.32202687_32202688delinsAG | GRCh38 |
NC_000006.11:g.32170464_32170465delinsAG , CM000668.1:g.32170464_32170465delinsAG | GRCh37 |
NC_000006.10:g.32278442_32278443delinsAG | NCBI36 |
NG_028190.1:g.26380_26381delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-89_3232-88delinsCT MANE Select | ENSP00000364163.3:n.3232-89_3232-88delinsCT | |
ENST00000474612.1:n.1229_1230delinsCT | ||
NM_004557.3:c.3232-89_3232-88delinsCT | NP_004548.3:n.3232-89_3232-88delinsCT | |
NR_134949.1:n.3472+1082_3472+1083delinsCT | ||
NR_134950.1:n.3370+1082_3370+1083delinsCT | ||
NM_004557.4:c.3232-89_3232-88delinsCT MANE Select | NP_004548.3:n.3232-89_3232-88delinsCT | |
NR_134949.2:n.3472+1082_3472+1083delinsCT | ||
NR_134950.2:n.3370+1082_3370+1083delinsCT |