HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29717524_29717527delinsCTTA , CM000664.2:g.29717524_29717527delinsCTTA | GRCh38 |
NC_000002.11:g.29940390_29940393delinsCTTA , CM000664.1:g.29940390_29940393delinsCTTA | GRCh37 |
NC_000002.10:g.29793894_29793897delinsCTTA | NCBI36 |
NG_009445.1:g.209040_209043delinsTAAG , LRG_488:g.209040_209043delinsTAAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389048.8:c.787+51_787+54delinsTAAG MANE Select | ENSP00000373700.3:n.787+51_787+54delinsTAAG | |
ENST00000389048.7:c.787+51_787+54delinsTAAG | ENSP00000373700.3:n.787+51_787+54delinsTAAG | |
ENST00000618119.4:c.-345+51_-345+54delinsTAAG | ENSP00000482733.1:n.-345+51_-345+54delinsTAAG | |
NM_004304.4:c.787+51_787+54delinsTAAG | NP_004295.2:n.787+51_787+54delinsTAAG | |
XR_001738688.2:n.1717+51_1717+54delinsTAAG | ||
NM_004304.5:c.787+51_787+54delinsTAAG MANE Select | NP_004295.2:n.787+51_787+54delinsTAAG |