Canonical Allele Identifier: CA1126734549
Gene: ROR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91757547_91757548del , CM000671.2:g.91757547_91757548del GRCh38
NC_000009.11:g.94519829_94519830del , CM000671.1:g.94519829_94519830del GRCh37
NC_000009.10:g.93559650_93559651del NCBI36
NG_008089.1:g.197615_197616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.187_188del MANE Select ENSP00000364860.3:p.Asn63PhefsTer29
ENST00000375708.3:c.187_188del ENSP00000364860.3:p.Asn63PhefsTer29
ENST00000375715.5:c.-234_-233del ENSP00000364867.1:n.-234_-233del
ENST00000495386.5:n.450_451del
ENST00000546883.1:n.389_390del
ENST00000548585.2:n.53_54del
ENST00000550066.5:n.655_656del
NM_004560.3:c.187_188del NP_004551.2:p.Asn63PhefsTer29
XM_005252008.3:c.-234_-233del XP_005252065.1:n.-234_-233del
XM_006717121.2:c.-234_-233del XP_006717184.1:n.-234_-233del
XM_011518721.1:c.-234_-233del XP_011517023.1:n.-234_-233del
NM_001318204.1:c.187_188del NP_001305133.1:p.Asn63PhefsTer29
XM_005252008.4:c.-234_-233del XP_005252065.1:n.-234_-233del
XM_006717121.3:c.-234_-233del XP_006717184.1:n.-234_-233del
XM_017014762.1:c.178_179del XP_016870251.1:p.Asn60PhefsTer29
XM_017014763.1:c.-234_-233del XP_016870252.1:n.-234_-233del
XR_001746315.1:n.430_431del
NM_004560.4:c.187_188del MANE Select NP_004551.2:p.Asn63PhefsTer29
NM_001318204.2:c.187_188del NP_001305133.1:p.Asn63PhefsTer29