HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551746_43551764del , CM000681.2:g.43551746_43551764del | GRCh38 |
NC_000019.9:g.44055898_44055916del , CM000681.1:g.44055898_44055916del | GRCh37 |
NC_000019.8:g.48747738_48747756del | NCBI36 |
NG_033799.1:g.28815_28833del , LRG_784:g.28815_28833del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1083-77_1083-59del MANE Select | ENSP00000262887.5:n.1083-77_1083-59del | |
ENST00000262887.9:c.1083-77_1083-59del | ENSP00000262887.4:n.1083-77_1083-59del | |
ENST00000543982.5:c.990-77_990-59del | ENSP00000443671.1:n.990-77_990-59del | |
ENST00000597811.5:c.693-77_693-59del | ||
NM_006297.2:c.1083-77_1083-59del , LRG_784t1:c.1083-77_1083-59del | NP_006288.2:n.1083-77_1083-59del | |
NM_006297.3:c.1083-77_1083-59del MANE Select | NP_006288.2:n.1083-77_1083-59del |