Canonical Allele Identifier: CA1621761198
Gene: RNF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.37386237T= , CM000668.2:g.37386237T= GRCh38
NC_000006.11:g.37354013T= , CM000668.1:g.37354013T= GRCh37
NC_000006.10:g.37461991T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000373479.9:c.1442-4505T= MANE Select ENSP00000362578.4:n.1442-4505T=
ENST00000229866.10:c.*1251-4505T= ENSP00000229866.6:n.*1251-4505T=
ENST00000373479.8:c.1442-4505T= ENSP00000362578.4:n.1442-4505T=
ENST00000469731.5:c.1237-4505T= ENSP00000418879.1:n.1237-4505T=
ENST00000498460.1:c.515-4505T=
NM_003958.3:c.1442-4505T= NP_003949.1:n.1442-4505T=
NM_183078.2:c.1237-4505T= NP_898901.1:n.1237-4505T=
NR_046399.1:n.1741-4505T=
XM_006715241.2:c.1352-4505T= XP_006715304.1:n.1352-4505T=
XM_006715242.2:c.1147-4505T= XP_006715305.1:n.1147-4505T=
XR_427853.2:n.1462-4505T=
XR_427854.2:n.1666-4505T=
XR_427855.2:n.1461-4505T=
XR_427857.2:n.1371-4505T=
XM_006715241.3:c.1352-4505T= XP_006715304.1:n.1352-4505T=
XM_006715242.3:c.1147-4505T= XP_006715305.1:n.1147-4505T=
XM_017011462.1:c.1271-4505T= XP_016866951.1:n.1271-4505T=
XM_017011463.1:c.1066-4505T= XP_016866952.1:n.1066-4505T=
XM_017011464.1:c.1033-4505T= XP_016866953.1:n.1033-4505T=
XR_001743731.2:n.1656-4505T=
XR_001743734.2:n.1739-4505T=
XR_427853.3:n.1451-4505T=
NM_003958.4:c.1442-4505T= MANE Select NP_003949.1:n.1442-4505T=
NM_183078.3:c.1237-4505T= NP_898901.1:n.1237-4505T=
NR_046399.2:n.1730-4505T=