Canonical Allele Identifier: CA3170845626

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91733301C= , CM000671.2:g.91733301C=	GRCh38
NC_000009.11:g.94495583C= , CM000671.1:g.94495583C=	GRCh37
NC_000009.10:g.93535404C=	NCBI36
NG_008089.1:g.221862G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.758G= MANE Select	NP_004551.2:p.Arg253=
ENST00000375708.4:c.758G= MANE Select	ENSP00000364860.3:p.Arg253=
NM_001318204.1:c.758G=	NP_001305133.1:p.Arg253=
NM_001318204.2:c.758G=	NP_001305133.1:p.Arg253=
NM_004560.3:c.758G=	NP_004551.2:p.Arg253=
ENST00000375708.3:c.758G=	ENSP00000364860.3:p.Arg253=
ENST00000375715.5:c.338G=	ENSP00000364867.1:p.Arg113=
ENST00000550066.5:n.1226G=
XM_005252008.3:c.338G=	XP_005252065.1:p.Arg113=
XM_005252008.4:c.338G=	XP_005252065.1:p.Arg113=
XM_006717121.2:c.338G=	XP_006717184.1:p.Arg113=
XM_006717121.3:c.338G=	XP_006717184.1:p.Arg113=
XM_011518721.1:c.338G=	XP_011517023.1:p.Arg113=
XM_017014762.1:c.749G=	XP_016870251.1:p.Arg250=
XM_017014763.1:c.338G=	XP_016870252.1:p.Arg113=
XR_001746315.1:n.1001G=