HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116172616dup , CM000685.2:g.116172616dup | GRCh38 |
NC_000023.10:g.115303869dup , CM000685.1:g.115303869dup | GRCh37 |
NC_000023.9:g.115217897dup | NCBI36 |
NG_016326.1:g.6912dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.336dup MANE Select | ENSP00000360973.4:p.Gly113TrpfsTer29 | |
ENST00000680409.1:n.804dup | ||
ENST00000681852.1:c.336dup | ENSP00000505750.1:p.Gly113TrpfsTer29 | |
ENST00000371906.4:c.336dup | ENSP00000360973.4:p.Gly113TrpfsTer29 | |
NM_000686.4:c.336dup | NP_000677.2:p.Gly113TrpfsTer29 | |
XM_011537533.1:c.336dup | XP_011535835.1:p.Gly113TrpfsTer29 | |
NM_000686.5:c.336dup MANE Select | NP_000677.2:p.Gly113TrpfsTer29 | |
NM_001385624.1:c.336dup | NP_001372553.1:p.Gly113TrpfsTer29 |