Canonical Allele Identifier: CA1863923143

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757260T= , CM000671.2:g.91757260T=	GRCh38
NC_000009.11:g.94519542T= , CM000671.1:g.94519542T=	GRCh37
NC_000009.10:g.93559363T=	NCBI36
NG_008089.1:g.197903A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.463+12A= MANE Select	ENSP00000364860.3:n.463+12A=
ENST00000375708.3:c.463+12A=	ENSP00000364860.3:n.463+12A=
ENST00000375715.5:c.43+12A=	ENSP00000364867.1:n.43+12A=
ENST00000548585.2:n.172+169A=
ENST00000550066.5:n.931+12A=
NM_004560.3:c.463+12A=	NP_004551.2:n.463+12A=
XM_005252008.3:c.43+12A=	XP_005252065.1:n.43+12A=
XM_006717121.2:c.43+12A=	XP_006717184.1:n.43+12A=
XM_011518721.1:c.43+12A=	XP_011517023.1:n.43+12A=
NM_001318204.1:c.463+12A=	NP_001305133.1:n.463+12A=
XM_005252008.4:c.43+12A=	XP_005252065.1:n.43+12A=
XM_006717121.3:c.43+12A=	XP_006717184.1:n.43+12A=
XM_017014762.1:c.454+12A=	XP_016870251.1:n.454+12A=
XM_017014763.1:c.43+12A=	XP_016870252.1:n.43+12A=
XR_001746315.1:n.706+12A=
NM_004560.4:c.463+12A= MANE Select	NP_004551.2:n.463+12A=
NM_001318204.2:c.463+12A=	NP_001305133.1:n.463+12A=