Canonical Allele Identifier: CA521017826

Gene: RNF207

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6210218_6210224del , CM000663.2:g.6210218_6210224del	GRCh38
NC_000001.10:g.6270278_6270284del , CM000663.1:g.6270278_6270284del	GRCh37
NC_000001.9:g.6192865_6192871del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_207396.2:c.801-5_802del
NM_207396.3:c.801-5_802del
ENST00000377939.4:c.801-5_802del
ENST00000377939.5:c.801-5_802del
ENST00000485539.5:n.810-5_811del
ENST00000496676.5:n.340-5_341del
XM_011541438.1:c.801-5_802del
XM_011541439.1:c.945-5_946del
XM_011541439.3:c.945-5_946del
XM_011541440.1:c.945-5_946del
XM_017001259.2:c.801-5_802del
XR_001737158.2:n.967-5_968del
XR_001737159.2:n.967-5_968del
XR_001737161.2:n.967-5_968del
XR_001737162.2:n.967-5_968del
XR_001737164.2:n.953-5_954del
XR_002956484.1:n.967-5_968del
XR_002956486.1:n.967-5_968del
XR_946651.1:n.1110-5_1111del
XR_946651.3:n.967-5_968del
XR_946652.1:n.1110-5_1111del
XR_946652.3:n.967-5_968del