HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322684dup , CM000677.2:g.73322684dup | GRCh38 |
NC_000015.9:g.73615025dup , CM000677.1:g.73615025dup | GRCh37 |
NC_000015.8:g.71402078dup | NCBI36 |
NG_009063.1:g.51585dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261917.4:c.3413dup MANE Select | ENSP00000261917.3:p.Gly1139TrpfsTer? | |
ENST00000261917.3:c.3413dup | ENSP00000261917.3:p.Gly1139TrpfsTer? | |
NM_005477.2:c.3413dup | NP_005468.1:p.Gly1139TrpfsTer? | |
XM_011521148.1:c.2195dup | XP_011519450.1:p.Gly733TrpfsTer? | |
XM_011521148.2:c.2195dup | XP_011519450.1:p.Gly733TrpfsTer? | |
NM_005477.3:c.3413dup MANE Select | NP_005468.1:p.Gly1139TrpfsTer? |