HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551899_43551900insG , CM000681.2:g.43551899_43551900insG | GRCh38 |
NC_000019.9:g.44056051_44056052insG , CM000681.1:g.44056051_44056052insG | GRCh37 |
NC_000019.8:g.48747891_48747892insG | NCBI36 |
NG_033799.1:g.28679_28680insC , LRG_784:g.28679_28680insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1082+117_1082+118insC MANE Select | ENSP00000262887.5:n.1082+117_1082+118insC | |
ENST00000262887.9:c.1082+117_1082+118insC | ENSP00000262887.4:n.1082+117_1082+118insC | |
ENST00000543982.5:c.989+117_989+118insC | ENSP00000443671.1:n.989+117_989+118insC | |
ENST00000597811.5:c.692+117_692+118insC | ||
NM_006297.2:c.1082+117_1082+118insC , LRG_784t1:c.1082+117_1082+118insC | NP_006288.2:n.1082+117_1082+118insC | |
NM_006297.3:c.1082+117_1082+118insC MANE Select | NP_006288.2:n.1082+117_1082+118insC |