Canonical Allele Identifier: CA1621761207

Gene: RNF8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37386264G= , CM000668.2:g.37386264G=	GRCh38
NC_000006.11:g.37354040G= , CM000668.1:g.37354040G=	GRCh37
NC_000006.10:g.37462018G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373479.9:c.1442-4478G= MANE Select	ENSP00000362578.4:n.1442-4478G=
ENST00000229866.10:c.*1251-4478G=	ENSP00000229866.6:n.*1251-4478G=
ENST00000373479.8:c.1442-4478G=	ENSP00000362578.4:n.1442-4478G=
ENST00000469731.5:c.1237-4478G=	ENSP00000418879.1:n.1237-4478G=
ENST00000498460.1:c.515-4478G=
NM_003958.3:c.1442-4478G=	NP_003949.1:n.1442-4478G=
NM_183078.2:c.1237-4478G=	NP_898901.1:n.1237-4478G=
NR_046399.1:n.1741-4478G=
XM_006715241.2:c.1352-4478G=	XP_006715304.1:n.1352-4478G=
XM_006715242.2:c.1147-4478G=	XP_006715305.1:n.1147-4478G=
XR_427853.2:n.1462-4478G=
XR_427854.2:n.1666-4478G=
XR_427855.2:n.1461-4478G=
XR_427857.2:n.1371-4478G=
XM_006715241.3:c.1352-4478G=	XP_006715304.1:n.1352-4478G=
XM_006715242.3:c.1147-4478G=	XP_006715305.1:n.1147-4478G=
XM_017011462.1:c.1271-4478G=	XP_016866951.1:n.1271-4478G=
XM_017011463.1:c.1066-4478G=	XP_016866952.1:n.1066-4478G=
XM_017011464.1:c.1033-4478G=	XP_016866953.1:n.1033-4478G=
XR_001743731.2:n.1656-4478G=
XR_001743734.2:n.1739-4478G=
XR_427853.3:n.1451-4478G=
NM_003958.4:c.1442-4478G= MANE Select	NP_003949.1:n.1442-4478G=
NM_183078.3:c.1237-4478G=	NP_898901.1:n.1237-4478G=
NR_046399.2:n.1730-4478G=