HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551788_43551795del , CM000681.2:g.43551788_43551795del | GRCh38 |
NC_000019.9:g.44055940_44055947del , CM000681.1:g.44055940_44055947del | GRCh37 |
NC_000019.8:g.48747780_48747787del | NCBI36 |
NG_033799.1:g.28795_28802del , LRG_784:g.28795_28802del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1083-97_1083-90del MANE Select | ENSP00000262887.5:n.1083-97_1083-90del | |
ENST00000262887.9:c.1083-97_1083-90del | ENSP00000262887.4:n.1083-97_1083-90del | |
ENST00000543982.5:c.990-97_990-90del | ENSP00000443671.1:n.990-97_990-90del | |
ENST00000597811.5:c.693-97_693-90del | ||
NM_006297.2:c.1083-97_1083-90del , LRG_784t1:c.1083-97_1083-90del | NP_006288.2:n.1083-97_1083-90del | |
NM_006297.3:c.1083-97_1083-90del MANE Select | NP_006288.2:n.1083-97_1083-90del |