Canonical Allele Identifier: CA2523750186

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757244_91757245dup , CM000671.2:g.91757244_91757245dup	GRCh38
NC_000009.11:g.94519526_94519527dup , CM000671.1:g.94519526_94519527dup	GRCh37
NC_000009.10:g.93559347_93559348dup	NCBI36
NG_008089.1:g.197918_197919dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.463+27_463+28dup MANE Select	ENSP00000364860.3:n.463+27_463+28dup
ENST00000375708.3:c.463+27_463+28dup	ENSP00000364860.3:n.463+27_463+28dup
ENST00000375715.5:c.43+27_43+28dup	ENSP00000364867.1:n.43+27_43+28dup
ENST00000548585.2:n.172+184_172+185dup
ENST00000550066.5:n.931+27_931+28dup
NM_004560.3:c.463+27_463+28dup	NP_004551.2:n.463+27_463+28dup
XM_005252008.3:c.43+27_43+28dup	XP_005252065.1:n.43+27_43+28dup
XM_006717121.2:c.43+27_43+28dup	XP_006717184.1:n.43+27_43+28dup
XM_011518721.1:c.43+27_43+28dup	XP_011517023.1:n.43+27_43+28dup
NM_001318204.1:c.463+27_463+28dup	NP_001305133.1:n.463+27_463+28dup
XM_005252008.4:c.43+27_43+28dup	XP_005252065.1:n.43+27_43+28dup
XM_006717121.3:c.43+27_43+28dup	XP_006717184.1:n.43+27_43+28dup
XM_017014762.1:c.454+27_454+28dup	XP_016870251.1:n.454+27_454+28dup
XM_017014763.1:c.43+27_43+28dup	XP_016870252.1:n.43+27_43+28dup
XR_001746315.1:n.706+27_706+28dup
NM_004560.4:c.463+27_463+28dup MANE Select	NP_004551.2:n.463+27_463+28dup
NM_001318204.2:c.463+27_463+28dup	NP_001305133.1:n.463+27_463+28dup