Canonical Allele Identifier: CA1863922894

Gene: ROR2

Linked Data

• dbSNP Id: rs1836936048

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724524_91724525insCT , CM000671.2:g.91724524_91724525insCT	GRCh38
NC_000009.11:g.94486806_94486807insCT , CM000671.1:g.94486806_94486807insCT	GRCh37
NC_000009.10:g.93526627_93526628insCT	NCBI36
NG_008089.1:g.230638_230639insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1969_1970insAG MANE Select	ENSP00000364860.3:p.Arg657GlnfsTer?
ENST00000375708.3:c.1969_1970insAG	ENSP00000364860.3:p.Arg657GlnfsTer?
ENST00000375715.5:c.1549_1550insAG	ENSP00000364867.1:p.Arg517GlnfsTer?
ENST00000550066.5:n.2437_2438insAG
NM_004560.3:c.1969_1970insAG	NP_004551.2:p.Arg657GlnfsTer?
XM_005252008.3:c.1549_1550insAG	XP_005252065.1:p.Arg517GlnfsTer?
XM_005252009.3:c.766_767insAG	XP_005252066.1:p.Arg256GlnfsTer?
XM_006717121.2:c.1549_1550insAG	XP_006717184.1:p.Arg517GlnfsTer?
XM_011518721.1:c.1549_1550insAG	XP_011517023.1:p.Arg517GlnfsTer?
XM_005252008.4:c.1549_1550insAG	XP_005252065.1:p.Arg517GlnfsTer?
XM_006717121.3:c.1549_1550insAG	XP_006717184.1:p.Arg517GlnfsTer?
XM_017014762.1:c.1960_1961insAG	XP_016870251.1:p.Arg654GlnfsTer?
XM_017014763.1:c.1549_1550insAG	XP_016870252.1:p.Arg517GlnfsTer?
NM_004560.4:c.1969_1970insAG MANE Select	NP_004551.2:p.Arg657GlnfsTer?