HGVS | Genome Assembly |
---|---|
NC_000001.11:g.11847647A>G , CM000663.2:g.11847647A>G | GRCh38 |
NC_000001.10:g.11907704A>G , CM000663.1:g.11907704A>G | GRCh37 |
NC_000001.9:g.11830291A>G | NCBI36 |
NG_012926.1:g.5137T>C , LRG_751:g.5137T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000400892.3:c.*2032A>G (CLCN6) | ENSP00000496938.1:n.*2032A>G | |
ENST00000446542.5:n.995A>G (NPPA-AS1) | ||
ENST00000376476.1:c.-27-208T>C (NPPA) | ENSP00000365659.1:n.-27-208T>C | |
ENST00000376480.7:c.38T>C (NPPA) MANE Select | ENSP00000365663.3:p.Leu13Pro | |
ENST00000610706.1:c.38T>C (NPPA) | ENSP00000483195.1:p.Leu13Pro | |
NM_006172.3:c.38T>C , LRG_751t1:c.38T>C (NPPA) | NP_006163.1:p.Leu13Pro | |
NM_006172.4:c.38T>C (NPPA) MANE Select | NP_006163.1:p.Leu13Pro |