Canonical Allele Identifier: CA1685038320
Gene: RNF216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5641549_5641551delinsTTG , CM000669.2:g.5641549_5641551delinsTTG GRCh38
NC_000007.13:g.5681180_5681182delinsTTG , CM000669.1:g.5681180_5681182delinsTTG GRCh37
NC_000007.12:g.5647706_5647708delinsTTG NCBI36
NG_029374.1:g.145180_145182delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000389902.8:c.2160-175_2160-173delinsCAA MANE Select ENSP00000374552.3:n.2160-175_2160-173delinsCAA
ENST00000389900.8:c.*1277-175_*1277-173delinsCAA ENSP00000374550.4:n.*1277-175_*1277-173delinsCAA
ENST00000389902.7:c.2160-175_2160-173delinsCAA ENSP00000374552.3:n.2160-175_2160-173delinsCAA
ENST00000425013.6:c.1989-175_1989-173delinsCAA ENSP00000404602.2:n.1989-175_1989-173delinsCAA
ENST00000469375.1:n.377-175_377-173delinsCAA
ENST00000484458.2:n.464-175_464-173delinsCAA
NM_207111.3:c.2160-175_2160-173delinsCAA NP_996994.1:n.2160-175_2160-173delinsCAA
NM_207116.2:c.1989-175_1989-173delinsCAA NP_996999.1:n.1989-175_1989-173delinsCAA
XM_005249785.2:c.2160-175_2160-173delinsCAA XP_005249842.1:n.2160-175_2160-173delinsCAA
XM_006715748.1:c.855-175_855-173delinsCAA XP_006715811.1:n.855-175_855-173delinsCAA
XM_011515434.1:c.2160-175_2160-173delinsCAA XP_011513736.1:n.2160-175_2160-173delinsCAA
XM_011515436.1:c.855-175_855-173delinsCAA XP_011513738.1:n.855-175_855-173delinsCAA
XM_011515436.2:c.855-175_855-173delinsCAA XP_011513738.1:n.855-175_855-173delinsCAA
XM_017012363.2:c.1989-175_1989-173delinsCAA XP_016867852.1:n.1989-175_1989-173delinsCAA
XM_024446805.1:c.2160-175_2160-173delinsCAA XP_024302573.1:n.2160-175_2160-173delinsCAA
XM_024446806.1:c.855-175_855-173delinsCAA XP_024302574.1:n.855-175_855-173delinsCAA
XM_024446807.1:c.855-175_855-173delinsCAA XP_024302575.1:n.855-175_855-173delinsCAA
NM_001377156.1:c.1989-175_1989-173delinsCAA NP_001364085.1:n.1989-175_1989-173delinsCAA
NM_207111.4:c.2160-175_2160-173delinsCAA MANE Select NP_996994.1:n.2160-175_2160-173delinsCAA
NM_207116.3:c.1989-175_1989-173delinsCAA NP_996999.1:n.1989-175_1989-173delinsCAA