HGVS | Genome Assembly |
---|---|
NC_000012.12:g.53973838_53973843dup , CM000674.2:g.53973838_53973843dup | GRCh38 |
NC_000012.11:g.54367622_54367627dup , CM000674.1:g.54367622_54367627dup | GRCh37 |
NC_000012.10:g.52653889_52653894dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243082.4:c.597_602dup (HOXC11) | ENSP00000243082.4:p.Ala201_Glu202insGluAla | |
ENST00000546378.1:c.597_602dup (HOXC11) MANE Select | ENSP00000446680.1:p.Ala201_Glu202insGluAla | |
NM_014212.3:c.597_602dup (HOXC11) | NP_055027.1:p.Ala201_Glu202insGluAla | |
NR_047517.1:n.59+1060_59+1065dup (HOTAIR) | ||
NM_014212.4:c.597_602dup (HOXC11) MANE Select | NP_055027.1:p.Ala201_Glu202insGluAla |