HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551768_43551787del , CM000681.2:g.43551768_43551787del | GRCh38 |
NC_000019.9:g.44055920_44055939del , CM000681.1:g.44055920_44055939del | GRCh37 |
NC_000019.8:g.48747760_48747779del | NCBI36 |
NG_033799.1:g.28804_28823del , LRG_784:g.28804_28823del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1083-88_1083-69del MANE Select | ENSP00000262887.5:n.1083-88_1083-69del | |
ENST00000262887.9:c.1083-88_1083-69del | ENSP00000262887.4:n.1083-88_1083-69del | |
ENST00000543982.5:c.990-88_990-69del | ENSP00000443671.1:n.990-88_990-69del | |
ENST00000597811.5:c.693-88_693-69del | ||
NM_006297.2:c.1083-88_1083-69del , LRG_784t1:c.1083-88_1083-69del | NP_006288.2:n.1083-88_1083-69del | |
NM_006297.3:c.1083-88_1083-69del MANE Select | NP_006288.2:n.1083-88_1083-69del |