HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10644959del , CM000682.2:g.10644959del | GRCh38 |
NC_000020.10:g.10625607del , CM000682.1:g.10625607del | GRCh37 |
NC_000020.9:g.10573607del | NCBI36 |
NG_007496.1:g.34090del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000254958.10:c.2250del MANE Select | ENSP00000254958.4:p.Asn751ThrfsTer? | |
ENST00000617965.2:n.2839del | ||
ENST00000254958.9:c.2250del | ENSP00000254958.4:p.Asn751ThrfsTer? | |
ENST00000423891.6:n.2116del | ||
ENST00000488480.2:n.647del | ||
NM_000214.2:c.2250del | NP_000205.1:p.Asn751ThrfsTer? | |
NM_000214.3:c.2250del MANE Select | NP_000205.1:p.Asn751ThrfsTer? |