Canonical Allele Identifier: CA1621757399
Gene: RNF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.37381159T= , CM000668.2:g.37381159T= GRCh38
NC_000006.11:g.37348935T= , CM000668.1:g.37348935T= GRCh37
NC_000006.10:g.37456913T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000373479.9:c.1246T= MANE Select ENSP00000362578.4:p.Leu416=
ENST00000229866.10:c.*1055T= ENSP00000229866.6:n.*1055T=
ENST00000373479.8:c.1246T= ENSP00000362578.4:p.Leu416=
ENST00000469731.5:c.1236+4126T= ENSP00000418879.1:n.1236+4126T=
ENST00000498460.1:c.514+4126T=
NM_003958.3:c.1246T= NP_003949.1:p.Leu416=
NM_183078.2:c.1236+4126T= NP_898901.1:n.1236+4126T=
NR_046399.1:n.1545T=
XM_006715241.2:c.1156T= XP_006715304.1:p.Leu386=
XM_006715242.2:c.1146+4126T= XP_006715305.1:n.1146+4126T=
XR_427852.1:n.1471T=
XR_427853.2:n.1461+4126T=
XR_427854.2:n.1470T=
XR_427855.2:n.1460+4126T=
XR_427856.1:n.1380T=
XR_427857.2:n.1370+4126T=
XM_006715241.3:c.1156T= XP_006715304.1:p.Leu386=
XM_006715242.3:c.1146+4126T= XP_006715305.1:n.1146+4126T=
XM_017011462.1:c.1075T= XP_016866951.1:p.Leu359=
XM_017011463.1:c.1065+4126T= XP_016866952.1:n.1065+4126T=
XM_017011464.1:c.1032+4126T= XP_016866953.1:n.1032+4126T=
XR_001743731.2:n.1460T=
XR_001743734.2:n.1543T=
XR_427853.3:n.1450+4126T=
NM_003958.4:c.1246T= MANE Select NP_003949.1:p.Leu416=
NM_183078.3:c.1236+4126T= NP_898901.1:n.1236+4126T=
NR_046399.2:n.1534T=