HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10644636_10644727del , CM000682.2:g.10644636_10644727del | GRCh38 |
NC_000020.10:g.10625284_10625375del , CM000682.1:g.10625284_10625375del | GRCh37 |
NC_000020.9:g.10573284_10573375del | NCBI36 |
NG_007496.1:g.34320_34411del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.2344+136_2344+227del MANE Select | ENSP00000254958.4:n.2344+136_2344+227del | |
ENST00000617965.2:n.2933+136_2933+227del | ||
ENST00000254958.9:c.2344+136_2344+227del | ENSP00000254958.4:n.2344+136_2344+227del | |
ENST00000423891.6:n.2210+136_2210+227del | ||
ENST00000488480.2:n.877_968del | ||
NM_000214.2:c.2344+136_2344+227del | NP_000205.1:n.2344+136_2344+227del | |
NM_000214.3:c.2344+136_2344+227del MANE Select | NP_000205.1:n.2344+136_2344+227del |