Canonical Allele Identifier: CA1863923256

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757391T= , CM000671.2:g.91757391T=	GRCh38
NC_000009.11:g.94519673T= , CM000671.1:g.94519673T=	GRCh37
NC_000009.10:g.93559494T=	NCBI36
NG_008089.1:g.197772A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.344A= MANE Select	ENSP00000364860.3:p.Glu115=
ENST00000375708.3:c.344A=	ENSP00000364860.3:p.Glu115=
ENST00000375715.5:c.-77A=	ENSP00000364867.1:n.-77A=
ENST00000495386.5:n.607A=
ENST00000548585.2:n.172+38A=
ENST00000550066.5:n.812A=
NM_004560.3:c.344A=	NP_004551.2:p.Glu115=
XM_005252008.3:c.-77A=	XP_005252065.1:n.-77A=
XM_006717121.2:c.-77A=	XP_006717184.1:n.-77A=
XM_011518721.1:c.-77A=	XP_011517023.1:n.-77A=
NM_001318204.1:c.344A=	NP_001305133.1:p.Glu115=
XM_005252008.4:c.-77A=	XP_005252065.1:n.-77A=
XM_006717121.3:c.-77A=	XP_006717184.1:n.-77A=
XM_017014762.1:c.335A=	XP_016870251.1:p.Glu112=
XM_017014763.1:c.-77A=	XP_016870252.1:n.-77A=
XR_001746315.1:n.587A=
NM_004560.4:c.344A= MANE Select	NP_004551.2:p.Glu115=
NM_001318204.2:c.344A=	NP_001305133.1:p.Glu115=