Canonical Allele Identifier: CA1863925566

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726614G= , CM000671.2:g.91726614G=	GRCh38
NC_000009.11:g.94488896G= , CM000671.1:g.94488896G=	GRCh37
NC_000009.10:g.93528717G=	NCBI36
NG_008089.1:g.228549C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.1313C= MANE Select	ENSP00000364860.3:p.Thr438=
ENST00000375708.3:c.1313C=	ENSP00000364860.3:p.Thr438=
ENST00000375715.5:c.893C=	ENSP00000364867.1:p.Thr298=
ENST00000550066.5:n.1781C=
NM_004560.3:c.1313C=	NP_004551.2:p.Thr438=
XM_005252008.3:c.893C=	XP_005252065.1:p.Thr298=
XM_005252009.3:c.110C=	XP_005252066.1:p.Thr37=
XM_006717121.2:c.893C=	XP_006717184.1:p.Thr298=
XM_011518721.1:c.893C=	XP_011517023.1:p.Thr298=
NM_001318204.1:c.1279C=	NP_001305133.1:p.His427=
XM_005252008.4:c.893C=	XP_005252065.1:p.Thr298=
XM_006717121.3:c.893C=	XP_006717184.1:p.Thr298=
XM_017014762.1:c.1304C=	XP_016870251.1:p.Thr435=
XM_017014763.1:c.893C=	XP_016870252.1:p.Thr298=
XR_001746315.1:n.1522C=
NM_004560.4:c.1313C= MANE Select	NP_004551.2:p.Thr438=
NM_001318204.2:c.1279C=	NP_001305133.1:p.His427=