HGVS | Genome Assembly |
---|---|
NC_000001.11:g.11847651_11847653del , CM000663.2:g.11847651_11847653del | GRCh38 |
NC_000001.10:g.11907708_11907710del , CM000663.1:g.11907708_11907710del | GRCh37 |
NC_000001.9:g.11830295_11830297del | NCBI36 |
NG_012926.1:g.5135_5137del , LRG_751:g.5135_5137del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000400892.3:c.*2036_*2038del (CLCN6) | ENSP00000496938.1:n.*2036_*2038del | |
ENST00000446542.5:n.999_1001del (NPPA-AS1) | ||
ENST00000376476.1:c.-27-210_-27-208del (NPPA) | ENSP00000365659.1:n.-27-210_-27-208del | |
ENST00000376480.7:c.36_38del (NPPA) MANE Select | ENSP00000365663.3:p.Leu13del | |
ENST00000610706.1:c.36_38del (NPPA) | ENSP00000483195.1:p.Leu13del | |
NM_006172.3:c.36_38del , LRG_751t1:c.36_38del (NPPA) | NP_006163.1:p.Leu13del | |
NM_006172.4:c.36_38del (NPPA) MANE Select | NP_006163.1:p.Leu13del |