Canonical Allele Identifier: CA1863921783

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723945T= , CM000671.2:g.91723945T=	GRCh38
NC_000009.11:g.94486227T= , CM000671.1:g.94486227T=	GRCh37
NC_000009.10:g.93526048T=	NCBI36
NG_008089.1:g.231218A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2549A= MANE Select	ENSP00000364860.3:p.Gln850=
ENST00000375708.3:c.2549A=	ENSP00000364860.3:p.Gln850=
ENST00000375715.5:c.1920+209A=	ENSP00000364867.1:n.1920+209A=
ENST00000550066.5:n.3017A=
NM_004560.3:c.2549A=	NP_004551.2:p.Gln850=
XM_005252008.3:c.2129A=	XP_005252065.1:p.Gln710=
XM_005252009.3:c.1346A=	XP_005252066.1:p.Gln449=
XM_006717121.2:c.2129A=	XP_006717184.1:p.Gln710=
XM_011518721.1:c.2129A=	XP_011517023.1:p.Gln710=
XM_005252008.4:c.2129A=	XP_005252065.1:p.Gln710=
XM_006717121.3:c.2129A=	XP_006717184.1:p.Gln710=
XM_017014762.1:c.2540A=	XP_016870251.1:p.Gln847=
XM_017014763.1:c.2129A=	XP_016870252.1:p.Gln710=
NM_004560.4:c.2549A= MANE Select	NP_004551.2:p.Gln850=