Canonical Allele Identifier: CA913185051
Gene: ROR2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91726564dup , CM000671.2:g.91726564dup GRCh38
NC_000009.11:g.94488846dup , CM000671.1:g.94488846dup GRCh37
NC_000009.10:g.93528667dup NCBI36
NG_008089.1:g.228602dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.1366dup MANE Select ENSP00000364860.3:p.Leu456ProfsTer3
ENST00000375708.3:c.1366dup ENSP00000364860.3:p.Leu456ProfsTer3
ENST00000375715.5:c.946dup ENSP00000364867.1:p.Leu316ProfsTer3
ENST00000550066.5:n.1834dup
NM_004560.3:c.1366dup NP_004551.2:p.Leu456ProfsTer3
XM_005252008.3:c.946dup XP_005252065.1:p.Leu316ProfsTer3
XM_005252009.3:c.163dup XP_005252066.1:p.Leu55ProfsTer3
XM_006717121.2:c.946dup XP_006717184.1:p.Leu316ProfsTer3
XM_011518721.1:c.946dup XP_011517023.1:p.Leu316ProfsTer3
NM_001318204.1:c.*33dup NP_001305133.1:n.*33dup
XM_005252008.4:c.946dup XP_005252065.1:p.Leu316ProfsTer3
XM_006717121.3:c.946dup XP_006717184.1:p.Leu316ProfsTer3
XM_017014762.1:c.1357dup XP_016870251.1:p.Leu453ProfsTer3
XM_017014763.1:c.946dup XP_016870252.1:p.Leu316ProfsTer3
XR_001746315.1:n.1575dup
NM_004560.4:c.1366dup MANE Select NP_004551.2:p.Leu456ProfsTer3
NM_001318204.2:c.*33dup NP_001305133.1:n.*33dup