HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225672dup , CM000668.2:g.3225672dup | GRCh38 |
NC_000006.11:g.3225906dup , CM000668.1:g.3225906dup | GRCh37 |
NC_000006.10:g.3170905dup | NCBI36 |
NG_016715.1:g.7068dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.422dup MANE Select | ENSP00000259818.6:p.Gly142ArgfsTer? | |
ENST00000680070.1:n.1352dup | ||
ENST00000681707.1:n.1249dup | ||
ENST00000681757.1:n.727dup | ||
ENST00000259818.7:c.422dup | ENSP00000259818.6:p.Gly142ArgfsTer? | |
ENST00000473006.1:n.539dup | ||
NM_178012.4:c.422dup | NP_821080.1:p.Gly142ArgfsTer? | |
XM_011514571.1:c.206dup | XP_011512873.1:p.Gly70ArgfsTer? | |
NM_178012.5:c.422dup MANE Select | NP_821080.1:p.Gly142ArgfsTer? |