HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81646299_81646300insACAC , CM000665.2:g.81646299_81646300insACAC | GRCh38 |
NC_000003.11:g.81695450_81695451insACAC , CM000665.1:g.81695450_81695451insACAC | GRCh37 |
NC_000003.10:g.81778140_81778141insACAC | NCBI36 |
NG_011810.1:g.120501_120502insGTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.782+92_782+93insGTGT MANE Select | ENSP00000410833.2:n.782+92_782+93insGTGT | |
ENST00000429644.6:c.782+92_782+93insGTGT | ENSP00000410833.2:n.782+92_782+93insGTGT | |
ENST00000489715.1:c.659+92_659+93insGTGT | ENSP00000419638.1:n.659+92_659+93insGTGT | |
ENST00000498468.1:n.332+92_332+93insGTGT | ||
NM_000158.3:c.782+92_782+93insGTGT | NP_000149.3:n.782+92_782+93insGTGT | |
NM_000158.4:c.782+92_782+93insGTGT MANE Select | NP_000149.4:n.782+92_782+93insGTGT |