Canonical Allele Identifier: CA1685038037
Gene: RNF216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5641297G= , CM000669.2:g.5641297G= GRCh38
NC_000007.13:g.5680928G= , CM000669.1:g.5680928G= GRCh37
NC_000007.12:g.5647454G= NCBI36
NG_029374.1:g.145434C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389902.8:c.2239C= MANE Select ENSP00000374552.3:p.Arg747=
ENST00000389900.8:c.*1356C= ENSP00000374550.4:n.*1356C=
ENST00000389902.7:c.2239C= ENSP00000374552.3:p.Arg747=
ENST00000425013.6:c.2068C= ENSP00000404602.2:p.Arg690=
ENST00000469375.1:n.456C=
NM_207111.3:c.2239C= NP_996994.1:p.Arg747=
NM_207116.2:c.2068C= NP_996999.1:p.Arg690=
XM_005249785.2:c.2239C= XP_005249842.1:p.Arg747=
XM_006715748.1:c.934C= XP_006715811.1:p.Arg312=
XM_011515434.1:c.2239C= XP_011513736.1:p.Arg747=
XM_011515436.1:c.934C= XP_011513738.1:p.Arg312=
XM_011515436.2:c.934C= XP_011513738.1:p.Arg312=
XM_017012363.2:c.2068C= XP_016867852.1:p.Arg690=
XM_024446805.1:c.2239C= XP_024302573.1:p.Arg747=
XM_024446806.1:c.934C= XP_024302574.1:p.Arg312=
XM_024446807.1:c.934C= XP_024302575.1:p.Arg312=
NM_001377156.1:c.2068C= NP_001364085.1:p.Arg690=
NM_207111.4:c.2239C= MANE Select NP_996994.1:p.Arg747=
NM_207116.3:c.2068C= NP_996999.1:p.Arg690=