HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551776_43551779del , CM000681.2:g.43551776_43551779del | GRCh38 |
NC_000019.9:g.44055928_44055931del , CM000681.1:g.44055928_44055931del | GRCh37 |
NC_000019.8:g.48747768_48747771del | NCBI36 |
NG_033799.1:g.28811_28814del , LRG_784:g.28811_28814del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1083-81_1083-78del MANE Select | ENSP00000262887.5:n.1083-81_1083-78del | |
ENST00000262887.9:c.1083-81_1083-78del | ENSP00000262887.4:n.1083-81_1083-78del | |
ENST00000543982.5:c.990-81_990-78del | ENSP00000443671.1:n.990-81_990-78del | |
ENST00000597811.5:c.693-81_693-78del | ||
NM_006297.2:c.1083-81_1083-78del , LRG_784t1:c.1083-81_1083-78del | NP_006288.2:n.1083-81_1083-78del | |
NM_006297.3:c.1083-81_1083-78del MANE Select | NP_006288.2:n.1083-81_1083-78del |