Canonical Allele Identifier: CA278868

Gene: ROR2

Linked Data

• ClinVar Variation Id: 7311
• ClinVar RCV Id: RCV000007734 ; RCV000007735
• dbSNP Id: rs863223290
• MyVariant Identifiers: chr9:g.94488884_94488888del (hg19) ; chr9:g.91726602_91726606del (hg38)
• PubMed: PMID:10986040

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726603_91726607del , CM000671.2:g.91726603_91726607del	GRCh38
NC_000009.11:g.94488885_94488889del , CM000671.1:g.94488885_94488889del	GRCh37
NC_000009.10:g.93528706_93528710del	NCBI36
NG_008089.1:g.228557_228561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1321_1325del MANE Select	ENSP00000364860.3:p.Arg441ThrfsTer16
ENST00000375708.3:c.1321_1325del	ENSP00000364860.3:p.Arg441ThrfsTer16
ENST00000375715.5:c.901_905del	ENSP00000364867.1:p.Arg301ThrfsTer16
ENST00000550066.5:n.1789_1793del
NM_004560.3:c.1321_1325del	NP_004551.2:p.Arg441ThrfsTer16
XM_005252008.3:c.901_905del	XP_005252065.1:p.Arg301ThrfsTer16
XM_005252009.3:c.118_122del	XP_005252066.1:p.Arg40ThrfsTer16
XM_006717121.2:c.901_905del	XP_006717184.1:p.Arg301ThrfsTer16
XM_011518721.1:c.901_905del	XP_011517023.1:p.Arg301ThrfsTer16
NM_001318204.1:c.1287_1291del	NP_001305133.1:p.Ser429ArgfsTer?
XM_005252008.4:c.901_905del	XP_005252065.1:p.Arg301ThrfsTer16
XM_006717121.3:c.901_905del	XP_006717184.1:p.Arg301ThrfsTer16
XM_017014762.1:c.1312_1316del	XP_016870251.1:p.Arg438ThrfsTer16
XM_017014763.1:c.901_905del	XP_016870252.1:p.Arg301ThrfsTer16
XR_001746315.1:n.1530_1534del
NM_004560.4:c.1321_1325del MANE Select	NP_004551.2:p.Arg441ThrfsTer16
NM_001318204.2:c.1287_1291del	NP_001305133.1:p.Ser429ArgfsTer?